| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015541.2 | 3814 | Missense Mutation | AAA,GAA | K1092E | NP_056356.2 |
| XM_011533578.1 | 3814 | Missense Mutation | AAA,GAA | K1044E | XP_011531880.1 |
| XM_011533579.2 | 3814 | Missense Mutation | AAA,GAA | K832E | XP_011531881.1 |
| XM_017006134.1 | 3814 | Missense Mutation | AAA,GAA | K1067E | XP_016861623.1 |
| XM_017006135.1 | 3814 | Missense Mutation | AAA,GAA | K866E | XP_016861624.1 |
| XM_017006136.1 | 3814 | Missense Mutation | AAA,GAA | K832E | XP_016861625.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001164796.1 | 3814 | Intron | NP_001158268.1 | ||
| NM_173471.3 | 3814 | Intron | NP_775742.4 | ||
| XM_006712956.1 | 3814 | Intron | XP_006713019.1 | ||
| XM_011533327.2 | 3814 | Intron | XP_011531629.1 | ||
| XM_011533328.1 | 3814 | Intron | XP_011531630.1 | ||
| XM_017005671.1 | 3814 | Intron | XP_016861160.1 | ||
| XM_017005672.1 | 3814 | Intron | XP_016861161.1 | ||
| XM_017005673.1 | 3814 | Intron | XP_016861162.1 | ||
| XM_017005674.1 | 3814 | Intron | XP_016861163.1 |