Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001256134.1 | 38 | Missense Mutation | CTG,GTG | L11V | NP_001243063.1 |
NM_003891.2 | 38 | Missense Mutation | CTG,GTG | L11V | NP_003882.1 |
XM_017020812.1 | 38 | Missense Mutation | CTG,GTG | L56V | XP_016876301.1 |
XM_017020813.1 | 38 | Missense Mutation | CTG,GTG | L11V | XP_016876302.1 |