| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_182495.5 | 895 | Intron | NP_872301.2 | ||
| XM_011542604.2 | 895 | Intron | XP_011540906.1 | ||
| XM_017017206.1 | 895 | Intron | XP_016872695.1 | ||
| XM_017017207.1 | 895 | Intron | XP_016872696.1 | ||
| XM_017017208.1 | 895 | Intron | XP_016872697.1 | ||
| XM_017017209.1 | 895 | Intron | XP_016872698.1 | ||
| XM_017017210.1 | 895 | Intron | XP_016872699.1 | ||
| XM_017017211.1 | 895 | Intron | XP_016872700.1 | ||
| XM_017017212.1 | 895 | Intron | XP_016872701.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001077639.1 | 895 | Missense Mutation | ACC,ATC | T393I | NP_001071107.1 |
| NM_017678.2 | 895 | Missense Mutation | ACC,ATC | T109I | NP_060148.2 |
| XM_006718865.3 | 895 | Intron | XP_006718928.1 | ||
| XM_011542881.2 | 895 | Missense Mutation | ACC,ATC | T393I | XP_011541183.1 |
| XM_011542882.2 | 895 | Missense Mutation | ACC,ATC | T324I | XP_011541184.1 |
| XM_011542883.2 | 895 | Intron | XP_011541185.1 |