| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_005294.2 | 7110 | Missense Mutation | ACC,ATC | T136I | NP_005285.1 |
| XM_005251933.3 | 7110 | Missense Mutation | ACC,ATC | T136I | XP_005251990.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_012197.3 | 7110 | Intron | NP_036329.3 | ||
| XM_011518440.2 | 7110 | Intron | XP_011516742.1 | ||
| XM_011518441.2 | 7110 | Intron | XP_011516743.1 | ||
| XM_011518442.2 | 7110 | Intron | XP_011516744.1 | ||
| XM_011518444.2 | 7110 | Intron | XP_011516746.1 | ||
| XM_017014567.1 | 7110 | Intron | XP_016870056.1 | ||
| XM_017014568.1 | 7110 | Intron | XP_016870057.1 | ||
| XM_017014569.1 | 7110 | Intron | XP_016870058.1 | ||
| XM_017014570.1 | 7110 | Intron | XP_016870059.1 |