Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_021800.2 | 327 | Missense Mutation | TGG,TGT | W129C | NP_068572.1 |
NM_201262.1 | 327 | Intron | NP_957714.1 | ||
XM_017016431.1 | 327 | Missense Mutation | TGG,TGT | W47C | XP_016871920.1 |
XM_017016432.1 | 327 | Missense Mutation | TGG,TGT | W47C | XP_016871921.1 |