| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001010978.3 | 459 | Missense Mutation | CCA,TCA | P172S | NP_001010978.2 |
| NM_001276392.1 | 459 | Missense Mutation | CCA,TCA | P133S | NP_001263321.1 |
| NM_001276393.1 | 459 | Missense Mutation | CCA,TCA | P129S | NP_001263322.1 |
| NM_001276394.1 | 459 | Missense Mutation | CCA,TCA | P83S | NP_001263323.1 |
| NM_001276395.1 | 459 | UTR 3 | NP_001263324.1 | ||
| XM_011541446.1 | 459 | Missense Mutation | CCA,TCA | P171S | XP_011539748.1 |
| XM_017001264.1 | 459 | Intron | XP_016856753.1 |