ENST00000324868.13:c.572G>A
MANE Select
|
ENSP00000320658.8:p.Gly191Asp
|
|
ENST00000324868.12:c.572G>A
|
ENSP00000320658.8:p.Gly191Asp
|
|
ENST00000548490.1:c.494G>A
|
ENSP00000447710.1:p.Gly165Asp
|
|
NM_001040436.2:c.572G>A
|
NP_001035526.1:p.Gly191Asp
|
|
XR_242891.3:n.659G>A
|
|
|
XR_242892.3:n.659G>A
|
|
|
XR_429036.1:n.659G>A
|
|
|
XR_931296.1:n.659G>A
|
|
|
XR_931297.1:n.659G>A
|
|
|
XR_931298.1:n.659G>A
|
|
|
XR_931299.1:n.659G>A
|
|
|
XR_001748730.2:n.1156G>A
|
|
|
XR_002957331.1:n.1156G>A
|
|
|
XR_242892.5:n.1156G>A
|
|
|
XR_931296.3:n.1156G>A
|
|
|
NM_001040436.3:c.572G>A
MANE Select
|
NP_001035526.1:p.Gly191Asp
|
|