Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_182577.2 | 638 | Missense Mutation | CGG,TGG | R278W | NP_872383.1 |
XM_005259545.4 | 638 | Missense Mutation | CGG,TGG | R170W | XP_005259602.1 |
XM_017026671.1 | 638 | Missense Mutation | CGG,TGG | R170W | XP_016882160.1 |