| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001251962.1 | 282 | Missense Mutation | CCT,CTT | P24L | NP_001238891.1 |
| NM_001251963.1 | 282 | Missense Mutation | CCT,CTT | P24L | NP_001238892.1 |
| NM_015595.3 | 282 | Missense Mutation | CCT,CTT | P24L | NP_056410.3 |
| XM_011512672.1 | 282 | Missense Mutation | CCT,CTT | P24L | XP_011510974.1 |
| XM_017006160.1 | 282 | Intron | XP_016861649.1 |