Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001317906.1 | 859 | Missense Mutation | CGT,TGT | R91C | NP_001304835.1 |
NM_001317907.1 | 859 | Missense Mutation | CGT,TGT | R106C | NP_001304836.1 |
NM_152562.3 | 859 | Missense Mutation | CGT,TGT | R106C | NP_689775.2 |
XM_006716294.2 | 859 | Missense Mutation | CGT,TGT | R111C | XP_006716357.1 |
XM_011544415.1 | 859 | Missense Mutation | CGT,TGT | R111C | XP_011542717.1 |
XM_011544416.2 | 859 | Missense Mutation | CGT,TGT | R111C | XP_011542718.1 |
XM_011544417.2 | 859 | Missense Mutation | CGT,TGT | R111C | XP_011542719.1 |
XM_011544418.1 | 859 | Missense Mutation | CGT,TGT | R106C | XP_011542720.1 |