| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001143774.1 | 274 | Intron | NP_001137246.1 | ||
| NM_032439.3 | 274 | Missense Mutation | CCC,GCC | P13A | NP_115815.2 |
| XM_011540275.2 | 274 | UTR 5 | XP_011538577.1 | ||
| XM_011540276.2 | 274 | Intron | XP_011538578.1 | ||
| XM_017016782.1 | 274 | Intron | XP_016872271.1 | ||
| XM_017016783.1 | 274 | Intron | XP_016872272.1 |