Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_007202.3 | 2142 | Silent Mutation | CCA,CCG | P655P | NP_009133.2 |
XM_006721432.3 | 2142 | Silent Mutation | CCA,CCG | P597P | XP_006721495.1 |
XM_017024071.1 | 2142 | Intron | XP_016879560.1 |