| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_017525.2 | 4438 | Missense Mutation | CCT,CGT | P1430R | NP_059995.2 |
| XM_011545155.2 | 4438 | Missense Mutation | CCT,CGT | P1448R | XP_011543457.1 |
| XM_011545156.2 | 4438 | Missense Mutation | CCT,CGT | P1441R | XP_011543458.1 |
| XM_011545157.2 | 4438 | Silent Mutation | CCC,CCG | P1415P | XP_011543459.1 |
| XM_011545158.2 | 4438 | Silent Mutation | CCC,CCG | P1415P | XP_011543460.1 |
| XM_011545159.2 | 4438 | Missense Mutation | CCT,CGT | P1448R | XP_011543461.1 |
| XM_011545160.2 | 4438 | Missense Mutation | CCT,CGT | P1350R | XP_011543462.1 |
| XM_011545161.2 | 4438 | Intron | XP_011543463.1 | ||
| XM_017017996.1 | 4438 | Missense Mutation | CCT,CGT | P1447R | XP_016873485.1 |
| XM_017017997.1 | 4438 | Intron | XP_016873486.1 | ||
| XM_017017998.1 | 4438 | Intron | XP_016873487.1 | ||
| XM_017017999.1 | 4438 | Missense Mutation | CCT,CGT | P744R | XP_016873488.1 |