Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001204103.1 | 478 | Missense Mutation | CCG,CTG | P25L | NP_001191032.1 |
NM_005155.6 | 478 | Missense Mutation | CCG,CTG | P25L | NP_005146.4 |
NM_138717.2 | 478 | Missense Mutation | CCG,CTG | P31L | NP_619731.2 |