Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001171905.1 | 142 | Missense Mutation | CTA,GTA | L23V | NP_001165376.1 |
NM_001171906.1 | 142 | Missense Mutation | CTA,GTA | L69V | NP_001165377.1 |
NM_152395.2 | 142 | Missense Mutation | CTA,GTA | L69V | NP_689608.2 |