Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_130446.2 | 1561 | Silent Mutation | CCC,CCG | P616P | NP_569713.2 |
XM_011513273.2 | 1561 | Silent Mutation | CCC,CCG | P489P | XP_011511575.1 |
XM_011513274.2 | 1561 | Intron | XP_011511576.1 |