Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001009992.1 | 5238 | Missense Mutation | TGC,TTC | C366F | NP_001009992.1 |
XM_017000301.1 | 5238 | Missense Mutation | TGC,TTC | C366F | XP_016855790.1 |
XM_017000302.1 | 5238 | Missense Mutation | TGC,TTC | C366F | XP_016855791.1 |