Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001007527.1 | 2932 | Missense Mutation | TGT,TTT | C692F | NP_001007528.1 |
XM_011514162.2 | 2932 | Missense Mutation | TGT,TTT | C692F | XP_011512464.1 |
XM_017010024.1 | 2932 | Missense Mutation | TGT,TTT | C471F | XP_016865513.1 |