Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000020.2 | 296 | Missense Mutation | TGG,TGT | W50C | NP_000011.2 |
NM_001077401.1 | 296 | Missense Mutation | TGG,TGT | W50C | NP_001070869.1 |
XM_005269235.2 | 296 | Missense Mutation | TGG,TGT | W50C | XP_005269292.1 |
XM_011539008.1 | 296 | Missense Mutation | TGG,TGT | W64C | XP_011537310.1 |