Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_052935.4 | 859 | Missense Mutation | CGG,TGG | R261W | NP_443167.4 |
XM_006721669.3 | 859 | Missense Mutation | CGG,TGG | R218W | XP_006721732.1 |
XM_006721670.3 | 859 | Missense Mutation | CGG,TGG | R218W | XP_006721733.1 |
XM_011524276.2 | 859 | Missense Mutation | CGG,TGG | R194W | XP_011522578.1 |
XM_011524277.2 | 859 | Missense Mutation | CGG,TGG | R186W | XP_011522579.1 |
XM_017024127.1 | 859 | UTR 3 | XP_016879616.1 |