| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_004951.4 | 974 | Missense Mutation | CAT,CGT | H267R | NP_004942.1 |
| XM_017020405.1 | 974 | Missense Mutation | CAT,CGT | H267R | XP_016875894.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001144072.1 | 974 | Intron | NP_001137544.1 | ||
| NM_177967.3 | 974 | Intron | NP_808882.1 | ||
| XM_006719948.3 | 974 | Intron | XP_006720011.1 | ||
| XM_011521082.2 | 974 | Intron | XP_011519384.1 | ||
| XM_011521083.2 | 974 | Intron | XP_011519385.1 | ||
| XM_011521084.2 | 974 | Intron | XP_011519386.1 | ||
| XM_017020553.1 | 974 | Intron | XP_016876042.1 |