| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001144026.2 | 1782 | Missense Mutation | CCC,CGC | P171R | NP_001137498.1 |
| NM_001144027.2 | 1782 | Intron | NP_001137499.1 | ||
| NM_001144028.2 | 1782 | Missense Mutation | CCC,CGC | P171R | NP_001137500.1 |
| NM_014434.3 | 1782 | Missense Mutation | CCC,CGC | P171R | NP_055249.1 |
| XM_011518545.1 | 1782 | Intron | XP_011516847.1 | ||
| XM_011518547.1 | 1782 | Missense Mutation | CCC,CGC | P102R | XP_011516849.1 |
| XM_011518548.2 | 1782 | UTR 5 | XP_011516850.1 | ||
| XM_017014626.1 | 1782 | Missense Mutation | CCC,CGC | P171R | XP_016870115.1 |
| XM_017014627.1 | 1782 | Missense Mutation | CCC,CGC | P171R | XP_016870116.1 |