| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001306146.1 | 1506 | Missense Mutation | CAT,CGT | H399R | NP_001293075.1 |
| NM_002112.3 | 1506 | Missense Mutation | CAT,CGT | H432R | NP_002103.2 |
| XM_017022094.1 | 1506 | Missense Mutation | CAT,CGT | H467R | XP_016877583.1 |
| XM_017022095.1 | 1506 | Missense Mutation | CAT,CGT | H434R | XP_016877584.1 |
| XM_017022096.1 | 1506 | Missense Mutation | CAT,CGT | H391R | XP_016877585.1 |
| XM_017022097.1 | 1506 | Missense Mutation | CAT,CGT | H388R | XP_016877586.1 |
| XM_017022098.1 | 1506 | Missense Mutation | CAT,CGT | H323R | XP_016877587.1 |
| XM_017022099.1 | 1506 | Intron | XP_016877588.1 |