Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001199975.2 | 424 | Missense Mutation | CCG,CTG | P37L | NP_001186904.1 |
NM_001254752.1 | 424 | Missense Mutation | CCG,CTG | P69L | NP_001241681.1 |
NM_006294.4 | 424 | Missense Mutation | CCG,CTG | P69L | NP_006285.1 |