| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001172105.1 | 160 | Intron | NP_001165576.1 | ||
| NM_017577.4 | 160 | Missense Mutation | CCA,TCA | P32S | NP_060047.3 |
| XM_005247546.2 | 160 | Missense Mutation | CCA,TCA | P32S | XP_005247603.1 |
| XM_005247547.1 | 160 | Missense Mutation | CCA,TCA | P32S | XP_005247604.1 |
| XM_011512930.1 | 160 | Missense Mutation | CCA,TCA | P22S | XP_011511232.1 |
| XM_011512931.1 | 160 | Intron | XP_011511233.1 | ||
| XM_017006646.1 | 160 | Missense Mutation | CCA,TCA | P32S | XP_016862135.1 |
| XM_017006647.1 | 160 | UTR 5 | XP_016862136.1 | ||
| XM_017006648.1 | 160 | Intron | XP_016862137.1 | ||
| XM_017006649.1 | 160 | Intron | XP_016862138.1 |