Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_032514.3 | 835 | Missense Mutation | TGC,TTC | C121F | NP_115903.1 |
NM_181509.2 | 835 | Missense Mutation | TGC,TTC | C125F | NP_852610.1 |
XM_011529083.2 | 835 | Missense Mutation | TGC,TTC | C223F | XP_011527385.1 |
XM_011529084.2 | 835 | Missense Mutation | TGC,TTC | C223F | XP_011527386.1 |
XM_011529085.2 | 835 | Missense Mutation | TGC,TTC | C182F | XP_011527387.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_080476.4 | 835 | Intron | NP_536724.1 | ||
XM_011528542.2 | 835 | Intron | XP_011526844.1 | ||
XM_017027664.1 | 835 | Intron | XP_016883153.1 | ||
XM_017027665.1 | 835 | Intron | XP_016883154.1 |