Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001907.2 | 682 | Missense Mutation | TGC,TTC | C220F | NP_001898.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006742.2 | 682 | Intron | NP_006733.1 |