| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_017525.2 | 4528 | Missense Mutation | GAC,GTC | D1460V | NP_059995.2 |
| XM_011545155.2 | 4528 | Missense Mutation | GAC,GTC | D1478V | XP_011543457.1 |
| XM_011545156.2 | 4528 | Missense Mutation | GAC,GTC | D1471V | XP_011543458.1 |
| XM_011545157.2 | 4528 | Silent Mutation | GGA,GGT | G1445G | XP_011543459.1 |
| XM_011545158.2 | 4528 | Silent Mutation | GGA,GGT | G1445G | XP_011543460.1 |
| XM_011545159.2 | 4528 | Missense Mutation | GAC,GTC | D1478V | XP_011543461.1 |
| XM_011545160.2 | 4528 | Missense Mutation | GAC,GTC | D1380V | XP_011543462.1 |
| XM_011545161.2 | 4528 | Intron | XP_011543463.1 | ||
| XM_017017996.1 | 4528 | Missense Mutation | GAC,GTC | D1477V | XP_016873485.1 |
| XM_017017997.1 | 4528 | Intron | XP_016873486.1 | ||
| XM_017017998.1 | 4528 | Intron | XP_016873487.1 | ||
| XM_017017999.1 | 4528 | Missense Mutation | GAC,GTC | D774V | XP_016873488.1 |