| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001317987.1 | 825 | Missense Mutation | CAC,CGC | H99R | NP_001304916.1 |
| NM_014443.2 | 825 | Missense Mutation | CAC,CGC | H151R | NP_055258.1 |
| XM_011537622.2 | 825 | Missense Mutation | CAC,CGC | H99R | XP_011535924.1 |
| XM_017009346.1 | 825 | Missense Mutation | CAC,CGC | H216R | XP_016864835.1 |
| XM_017009347.1 | 825 | Missense Mutation | CAC,CGC | H99R | XP_016864836.1 |
| XM_017009348.1 | 825 | Missense Mutation | CAC,CGC | H99R | XP_016864837.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001301054.1 | 825 | Intron | NP_001287983.1 | ||
| NM_001301057.1 | 825 | Intron | NP_001287986.1 | ||
| NM_024028.3 | 825 | Intron | NP_076933.3 | ||
| XM_011537680.1 | 825 | Intron | XP_011535982.1 | ||
| XM_011537681.1 | 825 | Intron | XP_011535983.1 | ||
| XM_011537682.2 | 825 | Intron | XP_011535984.1 |