Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001172663.1 | 200 | Silent Mutation | CCG,CCT | P42P | NP_001166134.1 |
NM_001172664.1 | 200 | Silent Mutation | CCG,CCT | P42P | NP_001166135.1 |
NM_001172665.1 | 200 | Silent Mutation | CCG,CCT | P42P | NP_001166136.1 |
NM_001172666.1 | 200 | Silent Mutation | CCG,CCT | P42P | NP_001166137.1 |
NM_021168.4 | 200 | Silent Mutation | CCG,CCT | P42P | NP_066991.3 |