Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001199746.1 | 966 | Silent Mutation | CCG,CCT | P113P | NP_001186675.1 |
NM_001199747.1 | 966 | Intron | NP_001186676.1 | ||
NM_019558.3 | 966 | Silent Mutation | CCG,CCT | P113P | NP_062458.1 |