Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_198560.2 | 1505 | Silent Mutation | CCC,CCT | P227P | NP_940962.1 |
XM_017006359.1 | 1505 | Silent Mutation | CCC,CCT | P227P | XP_016861848.1 |
XM_017006360.1 | 1505 | Intron | XP_016861849.1 |