| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001324307.1 | 151 | Intron | NP_001311236.1 | ||
| NM_001324308.1 | 151 | Intron | NP_001311237.1 | ||
| NM_002511.3 | 151 | Intron | NP_002502.2 | ||
| XM_011535846.1 | 151 | Intron | XP_011534148.1 | ||
| XM_017010901.1 | 151 | Intron | XP_016866390.1 | ||
| XM_017010902.1 | 151 | Intron | XP_016866391.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286371.1 | 151 | Missense Mutation | CCG,GCG | P9A | NP_001273300.1 |
| NM_001286372.1 | 151 | UTR 5 | NP_001273301.1 | ||
| NM_016485.4 | 151 | Missense Mutation | CCG,GCG | P9A | NP_057569.2 |