Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142798.2 | 322 | Silent Mutation | GTC,GTT | V67V | NP_001136270.1 |
NM_001142799.2 | 322 | Intron | NP_001136271.1 | ||
NM_174893.3 | 322 | Silent Mutation | GTC,GTT | V67V | NP_777553.1 |