| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001034836.1 | 692 | Intron | NP_001030008.1 | ||
| NM_001163120.1 | 692 | Intron | NP_001156592.1 | ||
| NM_001163121.1 | 692 | Missense Mutation | AGT,GGT | S215G | NP_001156593.1 |
| NM_001163122.1 | 692 | Missense Mutation | AGT,GGT | S192G | NP_001156594.1 |
| NM_001163124.1 | 692 | Intron | NP_001156596.1 | ||
| NM_001163125.1 | 692 | Intron | NP_001156597.1 | ||
| NM_001163130.1 | 692 | Missense Mutation | AGT,GGT | S225G | NP_001156602.1 |
| NM_145654.3 | 692 | Missense Mutation | AGT,GGT | S248G | NP_663629.1 |
| XM_011524509.2 | 692 | Intron | XP_011522811.1 | ||
| XM_011524510.2 | 692 | Intron | XP_011522812.1 |