| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001040451.2 | 329 | UTR 5 | NP_001035541.1 | ||
| NM_001040452.2 | 329 | UTR 5 | NP_001035542.1 | ||
| NM_025158.4 | 329 | Missense Mutation | TGC,TTC | C107F | NP_079434.3 |
| XM_005265993.4 | 329 | Intron | XP_005266050.1 | ||
| XM_006714921.3 | 329 | Missense Mutation | TGC,TTC | C107F | XP_006714984.2 |
| XM_006714922.3 | 329 | Intron | XP_006714985.1 | ||
| XM_017009891.1 | 329 | UTR 5 | XP_016865380.1 | ||
| XM_017009892.1 | 329 | Intron | XP_016865381.1 | ||
| XM_017009893.1 | 329 | Intron | XP_016865382.1 | ||
| XM_017009894.1 | 329 | UTR 5 | XP_016865383.1 | ||
| XM_017009895.1 | 329 | UTR 5 | XP_016865384.1 |