| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001009909.3 | 322 | Silent Mutation | CTA,CTG | L16L | NP_001009909.2 |
| NM_001252008.1 | 322 | UTR 5 | NP_001238937.1 | ||
| NM_001252010.1 | 322 | Silent Mutation | CTA,CTG | L16L | NP_001238939.1 |
| XM_011520056.2 | 322 | Missense Mutation | AGT,GGT | S144G | XP_011518358.1 |
| XM_017017648.1 | 322 | UTR 5 | XP_016873137.1 | ||
| XM_017017649.1 | 322 | UTR 5 | XP_016873138.1 | ||
| XM_017017650.1 | 322 | Silent Mutation | CTA,CTG | L16L | XP_016873139.1 |
| XM_017017651.1 | 322 | Silent Mutation | CTA,CTG | L16L | XP_016873140.1 |