Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001198568.1 | 3062 | Missense Mutation | CGC,TGC | R982C | NP_001185497.1 |
NM_001198592.1 | 3062 | Missense Mutation | CGC,TGC | R982C | NP_001185521.1 |
NM_139247.3 | 3062 | Missense Mutation | CGC,TGC | R982C | NP_640340.2 |