| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_138471.2 | 480 | Missense Mutation | CCG,CTG | P56L | NP_612480.1 |
| XM_005273782.2 | 480 | Missense Mutation | CCG,CTG | P56L | XP_005273839.1 |
| XM_005273783.2 | 480 | Missense Mutation | CCG,CTG | P56L | XP_005273840.1 |
| XM_006718437.1 | 480 | Missense Mutation | CCG,CTG | P56L | XP_006718500.1 |
| XM_011544770.1 | 480 | Missense Mutation | CCG,CTG | P56L | XP_011543072.1 |
| XM_011544771.1 | 480 | Missense Mutation | CCG,CTG | P56L | XP_011543073.1 |
| XM_011544772.1 | 480 | Missense Mutation | CCG,CTG | P56L | XP_011543074.1 |