Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001297658.1 | 688 | Missense Mutation | ACG,ATG | T19M | NP_001284587.1 |
NM_001297659.1 | 688 | Missense Mutation | ACG,ATG | T19M | NP_001284588.1 |
NM_001297660.1 | 688 | Missense Mutation | ACG,ATG | T19M | NP_001284589.1 |
NM_001297661.1 | 688 | Intron | NP_001284590.1 | ||
NM_005706.3 | 688 | Missense Mutation | ACG,ATG | T19M | NP_005697.2 |
XM_006718118.2 | 688 | Missense Mutation | ACG,ATG | T19M | XP_006718181.1 |
XM_011519830.2 | 688 | Missense Mutation | ACG,ATG | T19M | XP_011518132.1 |