| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001261392.1 | 1663 | Missense Mutation | CAT,CGT | H645R | NP_001248321.1 |
| NM_001261394.1 | 1663 | Missense Mutation | CAT,CGT | H621R | NP_001248323.1 |
| NM_024894.3 | 1663 | Missense Mutation | CAT,CGT | H671R | NP_079170.2 |
| XM_011510398.2 | 1663 | Missense Mutation | CAT,CGT | H521R | XP_011508700.1 |
| XM_011510399.2 | 1663 | Missense Mutation | CAT,CGT | H521R | XP_011508701.1 |
| XM_011510400.2 | 1663 | Intron | XP_011508702.1 | ||
| XM_011510402.2 | 1663 | Intron | XP_011508704.1 | ||
| XM_017004990.1 | 1663 | Missense Mutation | CAT,CGT | H346R | XP_016860479.1 |
| XM_017004991.1 | 1663 | Missense Mutation | CAT,CGT | H346R | XP_016860480.1 |