Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_019002.3 | 410 | Missense Mutation | TGC,TTC | C93F | NP_061875.2 |
XM_017004376.1 | 410 | Missense Mutation | TGC,TTC | C93F | XP_016859865.1 |
XM_017004377.1 | 410 | Missense Mutation | TGC,TTC | C93F | XP_016859866.1 |