| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001195626.1 | 377 | Missense Mutation | CTG,GTG | L10V | NP_001182555.1 |
| NM_001195627.1 | 377 | Missense Mutation | CTG,GTG | L10V | NP_001182556.1 |
| NM_001195628.1 | 377 | Missense Mutation | CTG,GTG | L10V | NP_001182557.1 |
| NM_001195630.1 | 377 | Missense Mutation | CTG,GTG | L10V | NP_001182559.1 |
| NM_001324296.1 | 377 | Missense Mutation | CTG,GTG | L10V | NP_001311225.1 |
| NM_001324297.1 | 377 | UTR 5 | NP_001311226.1 | ||
| NM_004641.3 | 377 | Missense Mutation | CTG,GTG | L10V | NP_004632.1 |