Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001297732.1 | 894 | Missense Mutation | CGT,TGT | R262C | NP_001284661.1 |
NM_001297733.1 | 894 | Missense Mutation | CGT,TGT | R110C | NP_001284662.1 |
NM_001300729.1 | 894 | Missense Mutation | CGT,TGT | R264C | NP_001287658.1 |
NM_173827.3 | 894 | Missense Mutation | CGT,TGT | R261C | NP_776188.1 |
XM_005265680.4 | 894 | Missense Mutation | CGT,TGT | R262C | XP_005265737.1 |
XM_011531878.2 | 894 | Missense Mutation | CGT,TGT | R111C | XP_011530180.1 |
XM_017008045.1 | 894 | Missense Mutation | CGT,TGT | R261C | XP_016863534.1 |