| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001278312.1 | 3928 | Missense Mutation | CAC,CGC | H1196R | NP_001265241.1 |
| NM_004298.3 | 3928 | Missense Mutation | CAC,CGC | H1201R | NP_004289.1 |
| NM_153485.2 | 3928 | Missense Mutation | CAC,CGC | H1260R | NP_705618.1 |
| XM_011514165.2 | 3928 | Intron | XP_011512467.1 |