Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001303457.1 | 3262 | Silent Mutation | CCC,CCT | P1052P | NP_001290386.1 |
NM_014657.2 | 3262 | Silent Mutation | CCC,CCT | P1052P | NP_055472.1 |
XM_011529114.1 | 3262 | Intron | XP_011527416.1 | ||
XM_017028148.1 | 3262 | Intron | XP_016883637.1 |