Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_017706.4 | 193 | Missense Mutation | CGG,TGG | R27W | NP_060176.2 |
XM_005268469.2 | 193 | Missense Mutation | CGG,TGG | R27W | XP_005268526.1 |
XM_017009600.1 | 193 | Intron | XP_016865089.1 |