Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_016538.2 | 2662 | Missense Mutation | TGC,TGG | C336W | NP_057622.1 |
XM_006722284.2 | 2662 | Missense Mutation | TGC,TGG | C254W | XP_006722347.1 |
XM_011523580.1 | 2662 | Missense Mutation | TGC,TGG | C301W | XP_011521882.1 |
XM_011523581.2 | 2662 | Missense Mutation | TGC,TGG | C265W | XP_011521883.1 |