| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001079692.2 | 653 | Missense Mutation | ACT,CCT | T30P | NP_001073160.1 |
| NM_001261827.1 | 653 | Missense Mutation | ACT,CCT | T30P | NP_001248756.1 |
| NM_001261828.1 | 653 | Missense Mutation | ACT,CCT | T30P | NP_001248757.1 |
| NM_032597.4 | 653 | Missense Mutation | ACT,CCT | T30P | NP_115986.3 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_021201.4 | 653 | Intron | NP_067024.1 | ||
| NM_206938.1 | 653 | Intron | NP_996821.1 | ||
| NM_206939.1 | 653 | Intron | NP_996822.1 | ||
| NM_206940.1 | 653 | Intron | NP_996823.1 |