| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001170961.1 | 3588 | Missense Mutation | ACC,AGC | T1185S | NP_001164432.1 |
| NM_001170962.1 | 3588 | Missense Mutation | ACC,AGC | T1171S | NP_001164433.1 |
| NM_001170963.1 | 3588 | Intron | NP_001164434.1 | ||
| NM_001555.4 | 3588 | Missense Mutation | ACC,AGC | T1180S | NP_001546.2 |
| NM_205833.3 | 3588 | Intron | NP_991402.1 | ||
| XM_011531330.1 | 3588 | Missense Mutation | ACC,AGC | T1185S | XP_011529632.1 |
| XM_011531333.1 | 3588 | Missense Mutation | ACC,AGC | T1102S | XP_011529635.1 |
| XM_011531334.1 | 3588 | Missense Mutation | ACC,AGC | T993S | XP_011529636.1 |