| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001920.4 | 1126 | Missense Mutation | CCT,CTT | P299L | NP_001911.1 |
| NM_133503.3 | 1126 | Missense Mutation | CCT,CTT | P299L | NP_598010.1 |
| NM_133504.3 | 1126 | Missense Mutation | CCT,CTT | P190L | NP_598011.1 |
| NM_133505.3 | 1126 | Missense Mutation | CCT,CTT | P152L | NP_598012.1 |
| NM_133506.3 | 1126 | Missense Mutation | CCT,CTT | P112L | NP_598013.1 |
| NM_133507.3 | 1126 | Silent Mutation | CCC,CCT | P74P | NP_598014.1 |
| XM_005268693.1 | 1126 | Missense Mutation | CCT,CTT | P299L | XP_005268750.1 |
| XM_006719270.1 | 1126 | Missense Mutation | CCT,CTT | P299L | XP_006719333.1 |
| XM_017018917.1 | 1126 | Missense Mutation | CCT,CTT | P299L | XP_016874406.1 |