| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_022481.5 | 3810 | Missense Mutation | CCC,CTC | P1438L | NP_071926.4 |
| XM_005268497.1 | 3810 | Missense Mutation | CCC,CTC | P1425L | XP_005268554.1 |
| XM_005268498.1 | 3810 | Missense Mutation | CCC,CTC | P1418L | XP_005268555.1 |
| XM_005268499.1 | 3810 | Missense Mutation | CCC,CTC | P1360L | XP_005268556.1 |
| XM_005268500.3 | 3810 | Intron | XP_005268557.1 | ||
| XM_006714792.1 | 3810 | Missense Mutation | CCC,CTC | P1367L | XP_006714855.1 |
| XM_011537677.2 | 3810 | Missense Mutation | CCC,CTC | P1243L | XP_011535979.1 |