Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_199046.2 | 386 | Missense Mutation | CCT,GCT | P117A | NP_950247.2 |
NM_199456.2 | 386 | Missense Mutation | CCT,GCT | P117A | NP_955535.2 |
XM_017023218.1 | 386 | Missense Mutation | CCT,GCT | P62A | XP_016878707.1 |