Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001005567.2 | 482 | Intron | NP_001005567.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001005163.2 | 482 | Missense Mutation | CGT,TGT | R154C | NP_001005163.1 |