| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_006235.2 | 2447 | Missense Mutation | CCG,CTG | P164L | NP_006226.2 |
| XM_005271593.1 | 2447 | Missense Mutation | CCG,CTG | P211L | XP_005271650.1 |
| XM_005271594.3 | 2447 | Missense Mutation | CCG,CTG | P211L | XP_005271651.1 |
| XM_006718859.1 | 2447 | Missense Mutation | CCG,CTG | P184L | XP_006718922.1 |
| XM_006718860.3 | 2447 | UTR 3 | XP_006718923.1 | ||
| XM_017017932.1 | 2447 | UTR 3 | XP_016873421.1 |