Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001289807.1 | 294 | Intron | NP_001276736.1 | ||
NM_001289808.1 | 294 | Intron | NP_001276737.1 | ||
NM_001885.2 | 294 | Intron | NP_001876.1 | ||
XM_011542608.1 | 294 | Intron | XP_011540910.1 | ||
XM_011542609.2 | 294 | Intron | XP_011540911.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001541.3 | 294 | Missense Mutation | CAT,CTT | H67L | NP_001532.1 |