| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001198558.1 | 152 | Missense Mutation | CTG,GTG | L29V | NP_001185487.1 |
| NM_014441.2 | 152 | Missense Mutation | CTG,GTG | L29V | NP_055256.1 |
| XM_006723146.3 | 152 | Missense Mutation | CTG,GTG | L29V | XP_006723209.1 |
| XM_011526730.2 | 152 | Missense Mutation | CTG,GTG | L29V | XP_011525032.1 |
| XM_011526732.2 | 152 | Missense Mutation | CTG,GTG | L29V | XP_011525034.1 |
| XM_017026595.1 | 152 | Missense Mutation | CTG,GTG | L29V | XP_016882084.1 |
| XM_017026596.1 | 152 | Missense Mutation | CTG,GTG | L29V | XP_016882085.1 |