| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_025235.3 | 682 | Missense Mutation | AAG,AAT | K118N | NP_079511.1 |
| XM_005270185.4 | 682 | Missense Mutation | AAG,AAT | K139N | XP_005270242.2 |
| XM_011540213.1 | 682 | Missense Mutation | AAG,AAT | K139N | XP_011538515.1 |
| XM_011540215.2 | 682 | Intron | XP_011538517.1 | ||
| XM_017016696.1 | 682 | Missense Mutation | AAG,AAT | K118N | XP_016872185.1 |
| XM_017016697.1 | 682 | Missense Mutation | AGG,ATG | R6M | XP_016872186.1 |
| XM_017016698.1 | 682 | Missense Mutation | AGG,ATG | R6M | XP_016872187.1 |
| XM_017016699.1 | 682 | Missense Mutation | AGG,ATG | R6M | XP_016872188.1 |
| XM_017016700.1 | 682 | UTR 5 | XP_016872189.1 | ||
| XM_017016701.1 | 682 | Missense Mutation | AAG,AAT | K139N | XP_016872190.1 |