Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001267584.1 | 1460 | Silent Mutation | CCC,CCT | P477P | NP_001254513.1 |
NM_014948.3 | 1460 | Missense Mutation | CCG,CTG | P479L | NP_055763.1 |
NM_199415.2 | 1460 | Missense Mutation | CCG,CTG | P425L | NP_955447.1 |