| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_006820.3 | 136 | Missense Mutation | CAT,CCT | H33P | NP_006811.2 |
| XM_005270391.3 | 136 | Intron | XP_005270448.1 | ||
| XM_005270392.4 | 136 | Intron | XP_005270449.1 | ||
| XM_005270393.4 | 136 | Intron | XP_005270450.1 | ||
| XM_006710304.3 | 136 | Intron | XP_006710367.1 | ||
| XM_011540539.2 | 136 | Missense Mutation | CAT,CCT | H33P | XP_011538841.1 |
| XM_017000120.1 | 136 | Intron | XP_016855609.1 |