Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_015658.3 | 1872 | Intron | NP_056473.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152486.2 | 1872 | Missense Mutation | CGG,TGG | R598W | NP_689699.2 |