Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_014716.3 | 1745 | Intron | NP_055531.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001002914.2 | 1745 | Missense Mutation | CGG,TGG | R231W | NP_001002914.1 |