| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001260497.1 | 2362 | UTR 3 | NP_001247426.1 | ||
| NM_001260498.1 | 2362 | Missense Mutation | CCG,CTG | P624L | NP_001247427.1 |
| NM_001260499.1 | 2362 | UTR 3 | NP_001247428.1 | ||
| NM_139136.3 | 2362 | UTR 3 | NP_631874.1 | ||
| NM_139137.3 | 2362 | UTR 3 | NP_631875.1 | ||
| NM_153748.2 | 2362 | UTR 3 | NP_715624.1 | ||
| XM_005268855.3 | 2362 | Missense Mutation | CCG,CTG | P569L | XP_005268912.1 |
| XM_006719382.3 | 2362 | UTR 3 | XP_006719445.1 | ||
| XM_006719383.3 | 2362 | UTR 3 | XP_006719446.1 | ||
| XM_006719384.3 | 2362 | UTR 3 | XP_006719447.1 | ||
| XM_006719385.3 | 2362 | UTR 3 | XP_006719448.1 | ||
| XM_006719390.3 | 2362 | Intron | XP_006719453.1 | ||
| XM_017019282.1 | 2362 | Intron | XP_016874771.1 |