| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_017741.3 | 319 | Intron | NP_060211.3 | ||
| XM_005248169.3 | 319 | Intron | XP_005248226.1 | ||
| XM_005248171.3 | 319 | Intron | XP_005248228.1 | ||
| XM_006713966.3 | 319 | Intron | XP_006714029.1 | ||
| XM_017008327.1 | 319 | Intron | XP_016863816.1 | ||
| XM_017008328.1 | 319 | Intron | XP_016863817.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_022346.4 | 319 | Missense Mutation | CAC,CAG | H18Q | NP_071741.2 |
| XM_011513876.2 | 319 | UTR 5 | XP_011512178.1 | ||
| XM_017008543.1 | 319 | Missense Mutation | CAC,CAG | H18Q | XP_016864032.1 |
| XM_017008544.1 | 319 | UTR 5 | XP_016864033.1 |