| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001122821.1 | 433 | Intron | NP_001116293.1 | ||
| NM_001248000.1 | 433 | Intron | NP_001234929.1 | ||
| NM_001248001.1 | 433 | Intron | NP_001234930.1 | ||
| NM_003011.3 | 433 | Missense Mutation | CTC,TTC | L13F | NP_003002.2 |
| XM_017015013.1 | 433 | Intron | XP_016870502.1 | ||
| XM_017015014.1 | 433 | Intron | XP_016870503.1 | ||
| XM_017015015.1 | 433 | Intron | XP_016870504.1 | ||
| XM_017015016.1 | 433 | Missense Mutation | CTC,TTC | L13F | XP_016870505.1 |