| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001318025.1 | 368 | Intron | NP_001304954.1 | ||
| NM_001318026.1 | 368 | Intron | NP_001304955.1 | ||
| NM_001318027.1 | 368 | Intron | NP_001304956.1 | ||
| NM_001318028.1 | 368 | Missense Mutation | ATG,GTG | M39V | NP_001304957.1 |
| NM_174907.3 | 368 | Intron | NP_777567.1 |