Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001852.3 | 2173 | Missense Mutation | CGC,TGC | R679C | NP_001843.1 |
XM_006710365.3 | 2173 | Missense Mutation | CGC,TGC | R679C | XP_006710428.1 |
XM_011540715.2 | 2173 | Missense Mutation | CGC,TGC | R589C | XP_011539017.1 |
XM_011540716.2 | 2173 | Missense Mutation | CGC,TGC | R589C | XP_011539018.1 |
XM_011540717.2 | 2173 | Missense Mutation | CGC,TGC | R498C | XP_011539019.1 |
XM_017000332.1 | 2173 | Missense Mutation | CGC,TGC | R683C | XP_016855821.1 |
XM_017000333.1 | 2173 | Missense Mutation | CGC,TGC | R585C | XP_016855822.1 |