| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001005184.1 | 29 | Missense Mutation | CAT,CGT | H10R | NP_001005184.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001005185.1 | 29 | Intron | NP_001005185.1 | ||
| XM_017000325.1 | 29 | Intron | XP_016855814.1 | ||
| XM_017000326.1 | 29 | Intron | XP_016855815.1 | ||
| XM_017000327.1 | 29 | Intron | XP_016855816.1 |