| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_080615.1 | 1721 | Missense Mutation | CGA,GGA | R339G | NP_542182.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001283035.1 | 1721 | Intron | NP_001269964.1 | ||
| NM_001283036.1 | 1721 | Intron | NP_001269965.1 | ||
| NM_001283037.1 | 1721 | Intron | NP_001269966.1 | ||
| NM_016407.4 | 1721 | Intron | NP_057491.2 | ||
| XM_017027872.1 | 1721 | Intron | XP_016883361.1 |