| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_030582.3 | 3500 | Missense Mutation | CAC,CGC | H1160R | NP_085059.2 |
| NM_130444.2 | 3500 | Missense Mutation | CAC,CGC | H1395R | NP_569711.2 |
| NM_130445.3 | 3500 | Missense Mutation | CAC,CGC | H980R | NP_569712.2 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001205206.1 | 3500 | Intron | NP_001192135.1 | ||
| NM_001205207.1 | 3500 | Intron | NP_001192136.1 | ||
| NM_194255.2 | 3500 | Intron | NP_919231.1 | ||
| XM_005261164.3 | 3500 | Intron | XP_005261221.1 | ||
| XM_011529696.2 | 3500 | Intron | XP_011527998.1 | ||
| XM_011529698.2 | 3500 | Intron | XP_011528000.1 | ||
| XM_011529700.2 | 3500 | Intron | XP_011528002.1 | ||
| XM_011529701.2 | 3500 | Intron | XP_011528003.1 | ||
| XM_011529702.2 | 3500 | Intron | XP_011528004.1 | ||
| XM_011529703.2 | 3500 | Intron | XP_011528005.1 | ||
| XM_011529704.2 | 3500 | Intron | XP_011528006.1 | ||
| XM_011529706.2 | 3500 | Intron | XP_011528008.1 | ||
| XM_011529709.2 | 3500 | Intron | XP_011528011.1 | ||
| XM_017028443.1 | 3500 | Intron | XP_016883932.1 | ||
| XM_017028444.1 | 3500 | Intron | XP_016883933.1 | ||
| XM_017028445.1 | 3500 | Intron | XP_016883934.1 | ||
| XM_017028446.1 | 3500 | Intron | XP_016883935.1 |