| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_020798.2 | 613 | Missense Mutation | CAC,CGC | H87R | NP_065849.1 |
| XM_011545187.2 | 613 | Intron | XP_011543489.1 | ||
| XM_011545188.2 | 613 | Intron | XP_011543490.1 | ||
| XM_017018052.1 | 613 | Missense Mutation | CAC,CGC | H87R | XP_016873541.1 |
| XM_017018053.1 | 613 | Intron | XP_016873542.1 |