| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001258452.1 | 611 | Intron | NP_001245381.1 | ||
| NM_001258453.1 | 611 | Intron | NP_001245382.1 | ||
| NM_032807.4 | 611 | Missense Mutation | CAC,CGC | H33R | NP_116196.3 |
| NM_178150.2 | 611 | Intron | NP_835363.1 | ||
| XM_011519748.2 | 611 | Missense Mutation | CAC,CGC | H33R | XP_011518050.1 |
| XM_017016842.1 | 611 | Missense Mutation | CAC,CGC | H33R | XP_016872331.1 |
| XM_017016843.1 | 611 | Missense Mutation | CAC,CGC | H33R | XP_016872332.1 |
| XM_017016844.1 | 611 | Intron | XP_016872333.1 | ||
| XM_017016845.1 | 611 | Missense Mutation | CAC,CGC | H33R | XP_016872334.1 |
| XM_017016846.1 | 611 | Intron | XP_016872335.1 |