Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001320546.1 | 652 | Missense Mutation | GTT,TTT | V207F | NP_001307475.1 |
NM_001320547.1 | 652 | Missense Mutation | GTT,TTT | V182F | NP_001307476.1 |
NM_018031.4 | 652 | Missense Mutation | GTT,TTT | V263F | NP_060501.3 |