Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004640.6 | 1699 | Missense Mutation | GTG,TTG | V391L | NP_004631.1 |
NM_080598.5 | 1699 | Missense Mutation | GTG,TTG | V391L | NP_542165.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001011700.2 | 1699 | Intron | NP_001011700.2 |