| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001184734.1 | 1351 | Missense Mutation | ACG,ATG | T372M | NP_001171663.1 |
| NM_001184735.1 | 1351 | Intron | NP_001171664.1 | ||
| NM_014010.4 | 1351 | Missense Mutation | ACG,ATG | T1269M | NP_054729.3 |
| NM_198186.3 | 1351 | Missense Mutation | ACG,ATG | T421M | NP_937829.3 |
| NM_198187.3 | 1351 | Missense Mutation | ACG,ATG | T372M | NP_937830.3 |
| NM_198188.2 | 1351 | Missense Mutation | ACG,ATG | T372M | NP_937831.1 |