Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001040192.2 | 1126 | Missense Mutation | CCT,CGT | P226R | NP_001035282.1 |
NM_001320746.1 | 1126 | Missense Mutation | CCT,CGT | P226R | NP_001307675.1 |
NM_017833.4 | 1126 | Missense Mutation | CCT,CGT | P226R | NP_060303.2 |