| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001252020.1 | 4714 | Missense Mutation | ACG,ATG | T1467M | NP_001238949.1 |
| NM_001252024.1 | 4714 | Missense Mutation | ACG,ATG | T1450M | NP_001238953.1 |
| NM_001252030.1 | 4714 | Intron | NP_001238959.1 | ||
| NM_002420.5 | 4714 | Missense Mutation | ACG,ATG | T1428M | NP_002411.3 |