| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001199865.1 | 3847 | Missense Mutation | TTA,TTC | L1221F | NP_001186794.1 |
| NM_001199866.1 | 3847 | Intron | NP_001186795.1 | ||
| NM_024704.4 | 3847 | Missense Mutation | TTA,TTC | L1272F | NP_078980.3 |
| XM_005260750.3 | 3847 | Intron | XP_005260807.1 | ||
| XM_005260751.4 | 3847 | Intron | XP_005260808.1 | ||
| XM_005260752.3 | 3847 | Intron | XP_005260809.1 | ||
| XM_005260753.3 | 3847 | Missense Mutation | TTA,TTC | L1283F | XP_005260810.1 |
| XM_005260754.3 | 3847 | Missense Mutation | TTA,TTC | L1253F | XP_005260811.1 |
| XM_005260755.3 | 3847 | Missense Mutation | TTA,TTC | L1232F | XP_005260812.1 |
| XM_006723588.3 | 3847 | Missense Mutation | TTA,TTC | L1242F | XP_006723651.1 |
| XM_017027926.1 | 3847 | Missense Mutation | TTA,TTC | L1231F | XP_016883415.1 |