Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001105539.2 | 1451 | Missense Mutation | CTG,GTG | L285V | NP_001099009.1 |
NM_001277145.1 | 1451 | Intron | NP_001264074.1 | ||
NM_023929.4 | 1451 | Missense Mutation | CTG,GTG | L285V | NP_076418.3 |