| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001277155.2 | 1768 | Intron | NP_001264084.1 | ||
| NM_152490.4 | 1768 | UTR 3 | NP_689703.1 | ||
| XM_006711749.3 | 1768 | Intron | XP_006711812.1 | ||
| XM_017000394.1 | 1768 | UTR 3 | XP_016855883.1 | ||
| XM_017000395.1 | 1768 | UTR 3 | XP_016855884.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001079515.2 | 1768 | Missense Mutation | CAT,CGT | H480R | NP_001072983.1 |
| NM_001287801.1 | 1768 | Missense Mutation | CAT,CGT | H531R | NP_001274730.1 |
| NM_001287802.1 | 1768 | Missense Mutation | CAT,CGT | H367R | NP_001274731.1 |
| NM_003193.4 | 1768 | Missense Mutation | CAT,CGT | H480R | NP_003184.1 |