Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001164737.1 | 1623 | Missense Mutation | CCG,CTG | P481L | NP_001158209.1 |
NM_001164738.1 | 1623 | Missense Mutation | CCG,CTG | P447L | NP_001158210.1 |
NM_001742.3 | 1623 | Missense Mutation | CCG,CTG | P447L | NP_001733.1 |