| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001323407.1 | 212 | Intron | NP_001310336.1 | ||
| NM_001323408.1 | 212 | Missense Mutation | CCA,GCA | P11A | NP_001310337.1 |
| NM_001323409.1 | 212 | Missense Mutation | CCA,GCA | P11A | NP_001310338.1 |
| NM_001323410.1 | 212 | Missense Mutation | CCA,GCA | P11A | NP_001310339.1 |
| NM_006814.4 | 212 | Missense Mutation | CCA,GCA | P11A | NP_006805.2 |
| NM_178578.3 | 212 | Missense Mutation | CCA,GCA | P11A | NP_848693.2 |