| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001201334.1 | 2178 | Missense Mutation | CCT,GCT | P589A | NP_001188263.1 |
| NM_001201335.1 | 2178 | Intron | NP_001188264.1 | ||
| NM_003203.4 | 2178 | Missense Mutation | CCT,GCT | P758A | NP_003194.3 |
| XM_005264520.3 | 2178 | Missense Mutation | CCT,GCT | P766A | XP_005264577.1 |
| XM_011533074.2 | 2178 | Missense Mutation | CCT,GCT | P683A | XP_011531376.1 |
| XM_011533075.1 | 2178 | Intron | XP_011531377.1 | ||
| XM_017004787.1 | 2178 | Intron | XP_016860276.1 | ||
| XM_017004788.1 | 2178 | Intron | XP_016860277.1 |