| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001320977.1 | 337 | Missense Mutation | CTG,GTG | L57V | NP_001307906.1 |
| NM_006122.3 | 337 | Missense Mutation | CTG,GTG | L57V | NP_006113.2 |
| XM_005254910.3 | 337 | Missense Mutation | CTG,GTG | L57V | XP_005254967.1 |
| XM_011521565.2 | 337 | Intron | XP_011519867.1 | ||
| XM_011521566.2 | 337 | Intron | XP_011519868.1 | ||
| XM_017022184.1 | 337 | Missense Mutation | CTG,GTG | L57V | XP_016877673.1 |
| XM_017022185.1 | 337 | Missense Mutation | CTG,GTG | L57V | XP_016877674.1 |