Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_206922.2 | 86 | Missense Mutation | TGC,TTC | C29F | NP_996805.2 |
XM_005249103.3 | 86 | Missense Mutation | TGC,TTC | C29F | XP_005249160.1 |
XM_011514609.2 | 86 | Missense Mutation | TGC,TTC | C29F | XP_011512911.1 |
XM_017010856.1 | 86 | Missense Mutation | TGC,TTC | C29F | XP_016866345.1 |
XM_017010857.1 | 86 | Missense Mutation | TGC,TTC | C29F | XP_016866346.1 |