Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001281834.1 | 1033 | Intron | NP_001268763.1 | ||
NM_001281835.1 | 1033 | Intron | NP_001268764.1 | ||
NM_001281836.1 | 1033 | Intron | NP_001268765.1 | ||
NM_001281837.1 | 1033 | Intron | NP_001268766.1 | ||
NM_001281838.1 | 1033 | Intron | NP_001268767.1 | ||
NM_001281853.1 | 1033 | Intron | NP_001268782.1 | ||
NM_145278.4 | 1033 | Intron | NP_660321.1 | ||
XM_017000399.1 | 1033 | Intron | XP_016855888.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_198074.4 | 1033 | Missense Mutation | CAG,CGG | Q224R | NP_932340.3 |