Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001205252.1 | 942 | Missense Mutation | CCG,CTG | P214L | NP_001192181.1 |
XM_017001286.1 | 942 | Missense Mutation | CCG,CTG | P214L | XP_016856775.1 |
XM_017001287.1 | 942 | Intron | XP_016856776.1 |