Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_016474.4 | 177 | Missense Mutation | TCC,TTC | S29F | NP_057558.3 |
XM_017006554.1 | 177 | Missense Mutation | TCC,TTC | S29F | XP_016862043.1 |
XM_017006555.1 | 177 | Missense Mutation | TCC,TTC | S29F | XP_016862044.1 |