| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001256766.1 | 1086 | Missense Mutation | CTG,GTG | L270V | NP_001243695.1 |
| NM_017814.2 | 1086 | Missense Mutation | CTG,GTG | L373V | NP_060284.1 |
| XM_011528117.2 | 1086 | Missense Mutation | CTG,GTG | L171V | XP_011526419.1 |
| XM_017026916.1 | 1086 | Missense Mutation | CTG,GTG | L348V | XP_016882405.1 |