Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001281528.1 | 847 | Intron | NP_001268457.1 | ||
NM_001281529.1 | 847 | Intron | NP_001268458.1 | ||
NM_006263.3 | 847 | Intron | NP_006254.1 | ||
NM_176783.2 | 847 | Missense Mutation | ACT,GCT | T248A | NP_788955.1 |