| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001114726.2 | 1640 | UTR 3 | NP_001108198.2 | ||
| NM_001174164.1 | 1640 | Missense Mutation | CCG,CTG | P826L | NP_001167635.1 |
| XM_005250342.3 | 1640 | Missense Mutation | CCG,CTG | P826L | XP_005250399.1 |
| XM_005250343.3 | 1640 | Missense Mutation | CCG,CTG | P826L | XP_005250400.1 |
| XM_006715985.3 | 1640 | Missense Mutation | CCG,CTG | P826L | XP_006716048.1 |
| XM_017012205.1 | 1640 | Missense Mutation | CCG,CTG | P826L | XP_016867694.1 |
| XM_017012206.1 | 1640 | UTR 3 | XP_016867695.1 |