| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000352.4 | 4862 | Missense Mutation | CAT,CGT | H1578R | NP_000343.2 |
| NM_001287174.1 | 4862 | Missense Mutation | CAT,CGT | H1579R | NP_001274103.1 |
| XM_011520331.2 | 4862 | Missense Mutation | CAT,CGT | H1578R | XP_011518633.1 |
| XM_017018197.1 | 4862 | Missense Mutation | CAT,CGT | H1601R | XP_016873686.1 |
| XM_017018198.1 | 4862 | Missense Mutation | CAT,CGT | H1600R | XP_016873687.1 |
| XM_017018199.1 | 4862 | Missense Mutation | CAT,CGT | H1600R | XP_016873688.1 |
| XM_017018200.1 | 4862 | Missense Mutation | CAT,CGT | H1577R | XP_016873689.1 |
| XM_017018201.1 | 4862 | Intron | XP_016873690.1 | ||
| XM_017018202.1 | 4862 | Missense Mutation | CAT,CGT | H1100R | XP_016873691.1 |
| XM_017018203.1 | 4862 | Intron | XP_016873692.1 | ||
| XM_017018204.1 | 4862 | Missense Mutation | CAT,CGT | H897R | XP_016873693.1 |