| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001264573.1 | 2526 | Missense Mutation | CAC,CGC | H798R | NP_001251503.1 |
| NM_001265577.1 | 2526 | Missense Mutation | CAC,CGC | H786R | NP_001252506.1 |
| XM_011524385.2 | 2526 | Missense Mutation | CAC,CGC | H807R | XP_011522687.1 |
| XM_011524386.2 | 2526 | Missense Mutation | CAC,CGC | H798R | XP_011522688.1 |
| XM_011524387.2 | 2526 | Missense Mutation | CAC,CGC | H798R | XP_011522689.1 |
| XM_011524388.2 | 2526 | Missense Mutation | CAC,CGC | H795R | XP_011522690.1 |
| XM_011524389.2 | 2526 | Missense Mutation | CAC,CGC | H807R | XP_011522691.1 |
| XM_011524390.2 | 2526 | Missense Mutation | CAC,CGC | H772R | XP_011522692.1 |
| XM_011524391.2 | 2526 | Intron | XP_011522693.1 |