Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001893.4 | 1559 | Intron | NP_001884.2 | ||
NM_139062.2 | 1559 | Missense Mutation | AGC,GGC | S408G | NP_620693.1 |
XM_005256336.3 | 1559 | Intron | XP_005256393.1 | ||
XM_005256337.4 | 1559 | Intron | XP_005256394.1 | ||
XM_017024199.1 | 1559 | Intron | XP_016879688.1 |