| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001256167.1 | 89 | Intron | NP_001243096.1 | ||
| NM_001256168.1 | 89 | Intron | NP_001243097.1 | ||
| NM_175888.3 | 89 | Missense Mutation | CCA,TCA | P10S | NP_787084.1 |
| XM_005265011.3 | 89 | Missense Mutation | CCA,TCA | P10S | XP_005265068.1 |
| XM_005265012.3 | 89 | Missense Mutation | CCA,TCA | P10S | XP_005265069.1 |
| XM_017006064.1 | 89 | Missense Mutation | CCA,TCA | P55S | XP_016861553.1 |
| XM_017006065.1 | 89 | Missense Mutation | CCA,TCA | P10S | XP_016861554.1 |
| XM_017006066.1 | 89 | UTR 5 | XP_016861555.1 | ||
| XM_017006067.1 | 89 | UTR 5 | XP_016861556.1 | ||
| XM_017006068.1 | 89 | UTR 5 | XP_016861557.1 | ||
| XM_017006069.1 | 89 | Intron | XP_016861558.1 |