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In conclusion, you also need to have decent hardware setup. In terms of the CPU, make sure you have at least an Intel Core i5 and a graphics card that has an ATI/nVidia Geforce GTX 560 or better. A CPU that is a 1.3 GHz or faster is recommended.
You may also have to figure out how to close down your current Windows and then start up the Windows and process that can continue to run.
If these solutions don’t work, the best thing to do is to return your product to Autodesk.
This is where Autodesk allows you to purchase a refund on your product. Autodesk then credits your credit card with a new Autodesk 2012 product key.
See also:

How to solve REG_E_KEYNOTREG error on Windows 8.1 after release of new version of Windows (x64) and Windows 8.1 update
Restore Autodesk 2013 products: Autodesk Activation Center

Characterization of SLC16A5 variants in a French pedigreed population including patients with non-syndromic hearing loss.
Recent genome-wide linkage analysis has identified linkage to the SLC16A5 locus on chromosome 21q22.3 in non-syndromic hearing loss. SLC16A5 is expressed in the stria vascularis and encodes an anion transporter implicated in hearing loss in mice. SLC16A5 consists of 2 linked exons of a single approximately 6.4 kb transcript that encodes a 1229-residue protein. A putative transcription start site has been determined approximately 200 bp upstream of exon 1. The SLC16A5 coding sequence was sequenced in a French population including 28 probands with congenital/non-syndromic hearing loss and their relatives with normal hearing. Sixteen individuals with hearing loss carried 8 known sequence variations. In 5 of the 8 variants, amino acid changes occurred in the second exon, the largest percentage (56%) of which affects amino acid residues highly conserved between the murine and human proteins. Three of these variants, Ala229Thr, Leu306Ile and Cys329Arg, are novel, and probably contribute to hearing loss. The F240L and I282V variants represent allelic variants, each of which was present in three affected individuals with hearing loss. SLC16A5 variants p.Lig113 and p.Pro