Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_173558.3 | 317 | Missense Mutation | CGG,TGG | R52W | NP_775829.2 |
XM_011514372.2 | 317 | Missense Mutation | CGG,TGG | R52W | XP_011512674.1 |
XM_011514373.2 | 317 | Missense Mutation | CGG,TGG | R52W | XP_011512675.1 |
XM_017010429.1 | 317 | Missense Mutation | CGG,TGG | R52W | XP_016865918.1 |