| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_002550.2 | 802 | Missense Mutation | ACC,GCC | T268A | NP_002541.2 |
| XM_017024695.1 | 802 | Intron | XP_016880184.1 | ||
| XM_017024696.1 | 802 | Intron | XP_016880185.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_002551.3 | 802 | Intron | NP_002542.3 | ||
| XM_017024697.1 | 802 | Intron | XP_016880186.1 | ||
| XM_017024698.1 | 802 | Intron | XP_016880187.1 |