| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001242636.1 | 245 | Intron | NP_001229565.1 | ||
| NM_001242637.1 | 245 | Missense Mutation | CCG,CTG | P18L | NP_001229566.1 |
| NM_001242638.1 | 245 | UTR 5 | NP_001229567.1 | ||
| NM_001242639.1 | 245 | Intron | NP_001229568.1 | ||
| NM_001297570.1 | 245 | Missense Mutation | CCG,CTG | P18L | NP_001284499.1 |
| NM_001297572.1 | 245 | UTR 5 | NP_001284501.1 | ||
| NM_139017.5 | 245 | Missense Mutation | CCG,CTG | P18L | NP_620586.3 |
| XM_011543142.2 | 245 | Intron | XP_011541444.1 | ||
| XM_011543143.2 | 245 | Intron | XP_011541445.1 | ||
| XM_011543144.2 | 245 | Intron | XP_011541446.1 | ||
| XM_011543145.2 | 245 | Intron | XP_011541447.1 |