| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001291807.1 | 2174 | Missense Mutation | ACT,GCT | T656A | NP_001278736.1 |
| NM_004460.3 | 2174 | Missense Mutation | ACT,GCT | T681A | NP_004451.2 |
| XM_011510796.2 | 2174 | Missense Mutation | ACT,GCT | T671A | XP_011509098.1 |
| XM_011510797.2 | 2174 | Intron | XP_011509099.1 | ||
| XM_017003585.1 | 2174 | Intron | XP_016859074.1 |