| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001114172.1 | 1432 | Missense Mutation | CCC,CTC | P444L | NP_001107644.1 |
| NM_001303427.1 | 1432 | Missense Mutation | CCC,CTC | P490L | NP_001290356.1 |
| NM_001303428.1 | 1432 | Missense Mutation | CCC,CTC | P461L | NP_001290357.1 |
| NM_001303429.1 | 1432 | Missense Mutation | CCC,CTC | P385L | NP_001290358.1 |
| NM_003629.3 | 1432 | Missense Mutation | CCC,CTC | P444L | NP_003620.3 |
| XM_017002614.1 | 1432 | Missense Mutation | CCC,CTC | P444L | XP_016858103.1 |