ENST00000697953.1:n.3244G>T
|
|
|
ENST00000698013.1:n.3356G>T
|
|
|
ENST00000698014.1:n.3579G>T
|
|
|
ENST00000698015.1:n.2672G>T
|
|
|
ENST00000698016.1:c.*796G>T
|
ENSP00000513502.1:n.*796G>T
|
|
ENST00000698017.1:n.2746G>T
|
|
|
ENST00000698018.1:n.2877G>T
|
|
|
ENST00000698019.1:n.3075G>T
|
|
|
ENST00000698020.1:n.2181G>T
|
|
|
ENST00000698021.1:c.2090G>T
|
|
|
ENST00000698022.1:c.*796G>T
|
ENSP00000513504.1:n.*796G>T
|
|
ENST00000698023.1:n.2775G>T
|
|
|
ENST00000698024.1:n.2637G>T
|
|
|
ENST00000698025.1:n.2797G>T
|
|
|
ENST00000698026.1:n.1688G>T
|
|
|
ENST00000698027.1:c.*1013G>T
|
ENSP00000513505.1:n.*1013G>T
|
|
ENST00000448276.7:c.*796G>T
MANE Select
|
ENSP00000392617.2:n.*796G>T
|
|
ENST00000448276.6:c.*796G>T
|
ENSP00000392617.2:n.*796G>T
|
|
ENST00000613943.4:c.2281G>T
|
ENSP00000483605.1:n.2281G>T
|
|
NM_001098426.1:c.*796G>T
|
NP_001091896.1:n.*796G>T
|
|
XM_005257604.2:c.*796G>T
|
XP_005257661.2:n.*796G>T
|
|
NM_001330439.1:c.*796G>T
|
NP_001317368.1:n.*796G>T
|
|
NM_001330440.1:c.*796G>T
|
NP_001317369.1:n.*796G>T
|
|
NM_001098426.2:c.*796G>T
MANE Select
|
NP_001091896.1:n.*796G>T
|
|
NM_001330440.2:c.*796G>T
|
NP_001317369.1:n.*796G>T
|
|