| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001080539.1 | 188 | Missense Mutation | CCA,CTA | P18L | NP_001074008.1 |
| XM_006712438.3 | 188 | Missense Mutation | CCA,CTA | P18L | XP_006712501.1 |
| XM_006712439.3 | 188 | Intron | XP_006712502.1 | ||
| XM_011510985.2 | 188 | Intron | XP_011509287.1 | ||
| XM_011510987.2 | 188 | Intron | XP_011509289.1 | ||
| XM_011510988.2 | 188 | Intron | XP_011509290.1 | ||
| XM_017003861.1 | 188 | Missense Mutation | CCA,CTA | P18L | XP_016859350.1 |
| XM_017003862.1 | 188 | Missense Mutation | CCA,CTA | P18L | XP_016859351.1 |
| XM_017003863.1 | 188 | Missense Mutation | CCA,CTA | P18L | XP_016859352.1 |
| XM_017003864.1 | 188 | Missense Mutation | CCA,CTA | P18L | XP_016859353.1 |
| XM_017003865.1 | 188 | Intron | XP_016859354.1 | ||
| XM_017003866.1 | 188 | Intron | XP_016859355.1 |