Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_016538.2 | 2768 | Missense Mutation | CGG,TGG | R372W | NP_057622.1 |
XM_006722284.2 | 2768 | Missense Mutation | CGG,TGG | R290W | XP_006722347.1 |
XM_011523580.1 | 2768 | Missense Mutation | CGG,TGG | R337W | XP_011521882.1 |
XM_011523581.2 | 2768 | Missense Mutation | CGG,TGG | R301W | XP_011521883.1 |