ENST00000242152.7:c.270-869A>G
MANE Select
|
ENSP00000242152.2:n.270-869A>G
|
|
ENST00000242152.6:c.270-869A>G
|
ENSP00000242152.2:n.270-869A>G
|
|
ENST00000405982.1:c.270-869A>G
|
ENSP00000385282.1:n.270-869A>G
|
|
ENST00000407573.5:c.270-869A>G
|
ENSP00000384364.1:n.270-869A>G
|
|
NM_000905.3:c.270-869A>G
|
NP_000896.1:n.270-869A>G
|
|
XM_017012910.1:c.41+28563T>C
|
XP_016868399.1:n.41+28563T>C
|
|
XM_017012911.1:c.41+28563T>C
|
XP_016868400.1:n.41+28563T>C
|
|
XR_001745121.1:n.473+28563T>C
|
|
|
XR_001745122.1:n.345-93765T>C
|
|
|
XR_001745123.1:n.473+28563T>C
|
|
|
XR_001745124.1:n.473+28563T>C
|
|
|
XR_001745125.1:n.473+28563T>C
|
|
|
XR_001745126.1:n.473+28563T>C
|
|
|
XR_001745127.1:n.345-35095T>C
|
|
|
XR_001745129.1:n.473+28563T>C
|
|
|
XR_001745130.1:n.473+28563T>C
|
|
|
XR_001745131.1:n.473+28563T>C
|
|
|
XR_001745132.1:n.473+28563T>C
|
|
|
NM_000905.4:c.270-869A>G
MANE Select
|
NP_000896.1:n.270-869A>G
|
|