| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145725.1 | 1129 | Missense Mutation | CTG,GTG | L319V | NP_001139197.1 |
| NM_017816.2 | 1129 | Missense Mutation | CTG,GTG | L319V | NP_060286.1 |
| XM_011513505.1 | 1129 | Missense Mutation | CTG,GTG | L319V | XP_011511807.1 |
| XM_011513506.2 | 1129 | Missense Mutation | CTG,GTG | L319V | XP_011511808.1 |