Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_144613.4 | 278 | Missense Mutation | TGC,TTC | C32F | NP_653214.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145402.1 | 278 | Intron | NP_001138874.1 |