| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001271052.1 | 2386 | Intron | NP_001257981.1 | ||
| NM_013447.3 | 2386 | Intron | NP_038475.2 | ||
| XM_011527948.2 | 2386 | Missense Mutation | CAA,GAA | Q832E | XP_011526250.1 |
| XM_011527949.2 | 2386 | Missense Mutation | CAA,GAA | Q821E | XP_011526251.1 |
| XM_011527951.2 | 2386 | Missense Mutation | CAA,GAA | Q783E | XP_011526253.1 |
| XM_011527952.2 | 2386 | Missense Mutation | CAA,GAA | Q774E | XP_011526254.1 |
| XM_011527953.2 | 2386 | Missense Mutation | CAA,GAA | Q739E | XP_011526255.1 |
| XM_011527954.2 | 2386 | Missense Mutation | CAA,GAA | Q719E | XP_011526256.1 |
| XM_011527955.2 | 2386 | Missense Mutation | CAA,GAA | Q633E | XP_011526257.1 |
| XM_017026726.1 | 2386 | Missense Mutation | CAA,GAA | Q793E | XP_016882215.1 |
| XM_017026727.1 | 2386 | Missense Mutation | CAA,GAA | Q714E | XP_016882216.1 |