Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000308.3 | 1418 | Intron | NP_000299.2 | ||
NM_001127695.2 | 1418 | Intron | NP_001121167.1 | ||
NM_001167594.2 | 1418 | Intron | NP_001161066.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001242920.1 | 1418 | Missense Mutation | CAA,CGA | Q374R | NP_001229849.1 |
NM_001242921.1 | 1418 | Missense Mutation | CAA,CGA | Q381R | NP_001229850.1 |
NM_006227.3 | 1418 | Missense Mutation | CAA,CGA | Q469R | NP_006218.1 |
NM_182676.2 | 1418 | Missense Mutation | CAA,CGA | Q417R | NP_872617.1 |