Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_024939.2 | 1776 | Missense Mutation | TCC,TTC | S563F | NP_079215.2 |
XM_005256153.4 | 1776 | Missense Mutation | TCC,TTC | S562F | XP_005256210.1 |
XM_006721273.3 | 1776 | Missense Mutation | TCC,TTC | S437F | XP_006721336.1 |
XM_011523338.2 | 1776 | Missense Mutation | TCC,TTC | S437F | XP_011521640.1 |