| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_152718.2 | 2544 | Missense Mutation | CCT,CTT | P891L | NP_689931.2 |
| XM_006718460.1 | 2544 | Missense Mutation | CCT,CTT | P883L | XP_006718523.1 |
| XM_006718462.1 | 2544 | Missense Mutation | CCT,CTT | P831L | XP_006718525.1 |
| XM_011544817.1 | 2544 | Missense Mutation | CCT,CTT | P793L | XP_011543119.1 |
| XM_017017340.1 | 2544 | Missense Mutation | CCT,CTT | P870L | XP_016872829.1 |
| XM_017017341.1 | 2544 | Missense Mutation | CCT,CTT | P848L | XP_016872830.1 |
| XM_017017342.1 | 2544 | Missense Mutation | CCT,CTT | P761L | XP_016872831.1 |
| XM_017017343.1 | 2544 | Missense Mutation | CCT,CTT | P608L | XP_016872832.1 |
| XM_017017344.1 | 2544 | Intron | XP_016872833.1 |