| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001199111.1 | 569 | Missense Mutation | CAC,CCC | H63P | NP_001186040.1 |
| NM_001199112.1 | 569 | Intron | NP_001186041.1 | ||
| NM_001316374.1 | 569 | Missense Mutation | CAC,CCC | H45P | NP_001303303.1 |
| NM_005917.3 | 569 | Missense Mutation | CAC,CCC | H45P | NP_005908.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001042692.2 | 569 | Intron | NP_001036157.1 | ||
| NM_015910.5 | 569 | Intron | NP_056994.3 | ||
| XM_005264348.3 | 569 | Intron | XP_005264405.1 | ||
| XM_011532881.2 | 569 | Intron | XP_011531183.1 | ||
| XM_011532884.2 | 569 | Intron | XP_011531186.1 | ||
| XM_011532886.2 | 569 | Intron | XP_011531188.1 | ||
| XM_011532887.2 | 569 | Intron | XP_011531189.1 | ||
| XM_011532890.2 | 569 | Intron | XP_011531192.1 | ||
| XM_011532891.2 | 569 | Intron | XP_011531193.1 | ||
| XM_017004251.1 | 569 | Intron | XP_016859740.1 | ||
| XM_017004252.1 | 569 | Intron | XP_016859741.1 | ||
| XM_017004253.1 | 569 | Intron | XP_016859742.1 | ||
| XM_017004254.1 | 569 | Intron | XP_016859743.1 |