| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001031723.3 | 1360 | Missense Mutation | CCT,CTT | P274L | NP_001026893.1 |
| NM_001278310.1 | 1360 | Missense Mutation | CCT,CTT | P207L | NP_001265239.1 |
| NM_001278311.1 | 1360 | Intron | NP_001265240.1 | ||
| XM_011532262.2 | 1360 | Missense Mutation | CCT,CTT | P189L | XP_011530564.1 |
| XM_011532263.2 | 1360 | Missense Mutation | CCT,CTT | P189L | XP_011530565.1 |
| XM_011532265.2 | 1360 | Missense Mutation | CCT,CTT | P186L | XP_011530567.1 |
| XM_017008628.1 | 1360 | Missense Mutation | CCT,CTT | P186L | XP_016864117.1 |