Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001303095.1 | 700 | Missense Mutation | CGG,TGG | R177W | NP_001290024.1 |
XM_005245516.4 | 700 | Missense Mutation | CGG,TGG | R177W | XP_005245573.1 |
XM_005245518.4 | 700 | Intron | XP_005245575.1 | ||
XM_006711560.3 | 700 | Missense Mutation | CGG,TGG | R177W | XP_006711623.1 |
XM_006711561.3 | 700 | Missense Mutation | CGG,TGG | R177W | XP_006711624.1 |