Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001004105.2 | 477 | Missense Mutation | ACG,ATG | T106M | NP_001004105.1 |
NM_001004106.2 | 477 | Missense Mutation | ACG,ATG | T106M | NP_001004106.1 |
NM_002082.3 | 477 | Missense Mutation | ACG,ATG | T106M | NP_002073.2 |
XM_006714858.3 | 477 | Missense Mutation | ACG,ATG | T76M | XP_006714921.1 |
XM_006714859.2 | 477 | Missense Mutation | ACG,ATG | T74M | XP_006714922.1 |
XM_011534537.2 | 477 | Missense Mutation | ACG,ATG | T67M | XP_011532839.1 |
XM_011534538.1 | 477 | Intron | XP_011532840.1 |