| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001278275.1 | 882 | Missense Mutation | CCA,TCA | P119S | NP_001265204.1 |
| NM_001278276.1 | 882 | Missense Mutation | CCA,TCA | P76S | NP_001265205.1 |
| NM_001278277.1 | 882 | Missense Mutation | CCA,TCA | P76S | NP_001265206.1 |
| NM_001278278.1 | 882 | Missense Mutation | CCA,TCA | P76S | NP_001265207.1 |
| NM_198256.3 | 882 | Missense Mutation | CCA,TCA | P151S | NP_937987.2 |
| NM_212540.2 | 882 | UTR 5 | NP_997705.1 | ||
| XM_017003547.1 | 882 | Missense Mutation | CCA,TCA | P151S | XP_016859036.1 |
| XM_017003548.1 | 882 | Missense Mutation | CCA,TCA | P119S | XP_016859037.1 |
| XM_017003549.1 | 882 | Missense Mutation | CCA,TCA | P76S | XP_016859038.1 |