| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001118.4 | 452 | Missense Mutation | CTG,GTG | L15V | NP_001109.2 |
| NM_001199635.1 | 452 | Missense Mutation | CTG,GTG | L15V | NP_001186564.1 |
| NM_001199636.1 | 452 | Missense Mutation | CTG,GTG | L15V | NP_001186565.1 |
| NM_001199637.1 | 452 | Missense Mutation | CTG,GTG | L15V | NP_001186566.1 |
| XM_005249618.4 | 452 | Missense Mutation | CTG,GTG | L15V | XP_005249675.1 |
| XM_006715645.2 | 452 | Missense Mutation | CTG,GTG | L15V | XP_006715708.1 |
| XM_017011736.1 | 452 | Missense Mutation | CTG,GTG | L15V | XP_016867225.1 |
| XM_017011737.1 | 452 | Missense Mutation | CTG,GTG | L15V | XP_016867226.1 |
| XM_017011738.1 | 452 | Missense Mutation | CTG,GTG | L15V | XP_016867227.1 |