| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142548.1 | 77 | Missense Mutation | CTG,GTG | L10V | NP_001136020.1 |
| NM_003579.3 | 77 | Missense Mutation | CTG,GTG | L10V | NP_003570.2 |
| XM_006710975.3 | 77 | UTR 5 | XP_006711038.1 | ||
| XM_011542299.2 | 77 | Intron | XP_011540601.1 | ||
| XM_011542300.2 | 77 | Intron | XP_011540602.1 |