Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001305942.1 | 556 | Intron | NP_001292871.1 | ||
NM_016035.4 | 556 | Missense Mutation | ATG,GTG | M69V | NP_057119.2 |
XM_017014792.1 | 556 | Intron | XP_016870281.1 | ||
XM_017014793.1 | 556 | Intron | XP_016870282.1 |