Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001172439.1 | 913 | Missense Mutation | CGC,TGC | R252C | NP_001165910.1 |
NM_001172440.1 | 913 | Missense Mutation | CGC,TGC | R189C | NP_001165911.1 |
NM_006025.3 | 913 | Missense Mutation | CGC,TGC | R211C | NP_006016.1 |