Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_174911.4 | 1058 | Missense Mutation | AGC,TGC | S177C | NP_777571.1 |
XM_017013107.1 | 1058 | Missense Mutation | AGC,TGC | S177C | XP_016868596.1 |
XM_017013108.1 | 1058 | Missense Mutation | AGC,TGC | S159C | XP_016868597.1 |