Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_030636.2 | 1088 | Missense Mutation | CCT,TCT | P124S | NP_085139.2 |
XM_017012657.1 | 1088 | Missense Mutation | CCT,TCT | P124S | XP_016868146.1 |
XM_017012658.1 | 1088 | Missense Mutation | CCT,TCT | P124S | XP_016868147.1 |