| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_013308.3 | 632 | Missense Mutation | GAC,GCC | D131A | NP_037440.3 |
| XM_005247402.3 | 632 | Missense Mutation | GAC,GCC | D131A | XP_005247459.1 |
| XM_005247403.3 | 632 | Missense Mutation | GAC,GCC | D131A | XP_005247460.1 |
| XM_017006274.1 | 632 | Missense Mutation | GAC,GCC | D131A | XP_016861763.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_053002.5 | 632 | Intron | NP_443728.3 | ||
| XM_006713487.3 | 632 | Intron | XP_006713550.1 | ||
| XM_011512390.2 | 632 | Intron | XP_011510692.1 | ||
| XM_011512394.2 | 632 | Intron | XP_011510696.1 | ||
| XM_011512399.2 | 632 | Intron | XP_011510701.1 | ||
| XM_017005676.1 | 632 | Intron | XP_016861165.1 | ||
| XM_017005677.1 | 632 | Intron | XP_016861166.1 | ||
| XM_017005678.1 | 632 | Intron | XP_016861167.1 | ||
| XM_017005679.1 | 632 | Intron | XP_016861168.1 | ||
| XM_017005680.1 | 632 | Intron | XP_016861169.1 | ||
| XM_017005681.1 | 632 | Intron | XP_016861170.1 |