Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_145807.2 | 871 | Missense Mutation | TGC,TGG | C221W | NP_665806.1 |
XM_011526443.2 | 871 | Missense Mutation | TGC,TGG | C221W | XP_011524745.1 |
XM_017026274.1 | 871 | Missense Mutation | TGC,TGG | C66W | XP_016881763.1 |