| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001010879.3 | 552 | Silent Mutation | CAA,CAT | Q70H | NP_001010879.2 |
| NM_001321145.1 | 552 | Silent Mutation | CAA,CAT | Q57H | NP_001308074.1 |
| NM_001321146.1 | 552 | Silent Mutation | CAA,CAT | Q15H | NP_001308075.1 |
| NM_001321147.1 | 552 | UTR 5 | NP_001308076.1 | ||
| XM_011526761.1 | 552 | Missense Mutation | CAA,CAT | Q56H | XP_011525063.1 |
| XM_011526762.1 | 552 | Missense Mutation | CAA,CAT | Q51H | XP_011525064.1 |
| XM_011526763.1 | 552 | Missense Mutation | CAA,CAT | Q43H | XP_011525065.1 |
| XM_011526764.1 | 552 | Missense Mutation | CAA,CAT | Q37H | XP_011525066.1 |
| XM_011526765.2 | 552 | Missense Mutation | CAA,CAT | Q34H | XP_011525067.1 |
| XM_011526766.2 | 552 | Missense Mutation | CAA,CAT | Q15H | XP_011525068.1 |
| XM_011526767.2 | 552 | UTR 5 | XP_011525069.1 |