| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001207012.1 | 972 | Intron | NP_001193941.1 | ||
| NM_001293643.1 | 972 | Missense Mutation | AGC,AGG | S149R | NP_001280572.1 |
| NM_002632.5 | 972 | Missense Mutation | AGC,AGG | S150R | NP_002623.2 |