| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001008779.1 | 859 | Intron | NP_001008779.1 | ||
| NM_001142634.1 | 859 | Intron | NP_001136106.1 | ||
| NM_182756.3 | 859 | Intron | NP_877433.2 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_017910.3 | 859 | Missense Mutation | CAC,CGC | H374R | NP_060380.3 |
| XM_005264393.2 | 859 | Missense Mutation | CAC,CGC | H374R | XP_005264450.1 |
| XM_006712037.2 | 859 | Missense Mutation | CAC,CGC | H276R | XP_006712100.1 |
| XM_017004401.1 | 859 | Missense Mutation | CAC,CGC | H276R | XP_016859890.1 |
| XM_017004402.1 | 859 | Intron | XP_016859891.1 | ||
| XM_017004403.1 | 859 | Missense Mutation | CAC,CGC | H138R | XP_016859892.1 |