| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001278312.1 | 4131 | Missense Mutation | CAT,GAT | H1264D | NP_001265241.1 |
| NM_004298.3 | 4131 | Missense Mutation | CAT,GAT | H1269D | NP_004289.1 |
| NM_153485.2 | 4131 | Missense Mutation | CAT,GAT | H1328D | NP_705618.1 |
| XM_011514165.2 | 4131 | Intron | XP_011512467.1 |