| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145029.1 | 570 | Missense Mutation | GAT,GGT | D162G | NP_001138501.1 |
| XM_006722325.3 | 570 | Intron | XP_006722388.1 | ||
| XM_011525662.2 | 570 | Missense Mutation | GAT,GGT | D162G | XP_011523964.1 |
| XM_011525664.2 | 570 | Intron | XP_011523966.1 | ||
| XM_011525665.2 | 570 | Missense Mutation | GAT,GGT | D162G | XP_011523967.1 |
| XM_011525666.2 | 570 | Missense Mutation | GAT,GGT | D162G | XP_011523968.1 |