Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001024649.1 | 400 | Intron | NP_001019820.1 | ||
NM_001746.3 | 400 | Intron | NP_001737.1 | ||
XM_011534664.1 | 400 | Missense Mutation | ACG,ATG | T7M | XP_011532966.1 |
XM_011534665.2 | 400 | Intron | XP_011532967.1 |