| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001270409.1 | 1302 | Missense Mutation | CAA,CCA | Q409P | NP_001257338.1 |
| NM_001270410.1 | 1302 | Missense Mutation | CAA,CCA | Q376P | NP_001257339.1 |
| NM_173083.3 | 1302 | Missense Mutation | CAA,CCA | Q444P | NP_775106.2 |
| XM_005273102.3 | 1302 | Missense Mutation | CAA,CCA | Q501P | XP_005273159.1 |
| XM_006711766.2 | 1302 | Missense Mutation | CAA,CCA | Q410P | XP_006711829.2 |
| XM_006711767.3 | 1302 | Missense Mutation | CAA,CCA | Q376P | XP_006711830.1 |
| XM_011544173.2 | 1302 | Intron | XP_011542475.1 | ||
| XM_017001084.1 | 1302 | Missense Mutation | CAA,CCA | Q432P | XP_016856573.1 |