Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001177675.1 | 996 | Missense Mutation | CCG,CTG | P288L | NP_001171146.1 |
NM_138814.3 | 996 | Missense Mutation | CCG,CTG | P402L | NP_620169.1 |
XM_011529959.2 | 996 | Missense Mutation | CCG,CTG | P262L | XP_011528261.1 |