| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_004210.4 | 551 | Missense Mutation | CAC,CGC | H18R | NP_004201.3 |
| XM_005270269.3 | 551 | Intron | XP_005270326.1 | ||
| XM_005270270.3 | 551 | Intron | XP_005270327.1 | ||
| XM_011540331.2 | 551 | Missense Mutation | CAC,CGC | H18R | XP_011538633.1 |
| XM_011540332.2 | 551 | Intron | XP_011538634.1 | ||
| XM_011540333.2 | 551 | Intron | XP_011538635.1 | ||
| XM_011540335.2 | 551 | Missense Mutation | CAC,CGC | H18R | XP_011538637.1 |
| XM_017016909.1 | 551 | Intron | XP_016872398.1 |