| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001111307.1 | 206 | Missense Mutation | CAC,CGC | H62R | NP_001104777.1 |
| NM_001111308.1 | 206 | Intron | NP_001104778.1 | ||
| NM_001111309.1 | 206 | Intron | NP_001104779.1 | ||
| NM_001243121.1 | 206 | Intron | NP_001230050.1 | ||
| NM_006202.2 | 206 | Intron | NP_006193.1 | ||
| XM_005259933.2 | 206 | Intron | XP_005259990.1 | ||
| XM_011528054.1 | 206 | Intron | XP_011526356.1 | ||
| XM_011528055.2 | 206 | Missense Mutation | CAC,CGC | H62R | XP_011526357.1 |
| XM_017026865.1 | 206 | Missense Mutation | CAC,CGC | H62R | XP_016882354.1 |