| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001001551.3 | 492 | Intron | NP_001001551.2 | ||
| NM_001256915.1 | 492 | Intron | NP_001243844.1 | ||
| XM_006717110.3 | 492 | Intron | XP_006717173.1 | ||
| XM_006717111.3 | 492 | Intron | XP_006717174.1 | ||
| XM_017014719.1 | 492 | Intron | XP_016870208.1 | ||
| XM_017014720.1 | 492 | Intron | XP_016870209.1 | ||
| XM_017014721.1 | 492 | Missense Mutation | GAT,GGT | D16G | XP_016870210.1 |
| XM_017014722.1 | 492 | Missense Mutation | GAT,GGT | D16G | XP_016870211.1 |
| XM_017014723.1 | 492 | Missense Mutation | GAT,GGT | D16G | XP_016870212.1 |
| XM_017014724.1 | 492 | Intron | XP_016870213.1 | ||
| XM_017014725.1 | 492 | Intron | XP_016870214.1 |