Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_019607.2 | 296 | Missense Mutation | CGG,TGG | R27W | NP_062553.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001204173.1 | 296 | Intron | NP_001191102.1 |