ENST00000303927.4:c.384+230T>C
MANE Select
|
ENSP00000307292.3:n.384+230T>C
|
|
ENST00000303927.3:c.384+230T>C
|
ENSP00000307292.3:n.384+230T>C
|
|
ENST00000524852.1:n.64-192T>C
|
|
|
ENST00000530979.1:c.385-111T>C
|
ENSP00000432047.1:n.385-111T>C
|
|
ENST00000532354.1:n.200T>C
|
|
|
NM_145040.2:c.384+230T>C
|
NP_659477.2:n.384+230T>C
|
|
XR_242848.3:n.136+166A>G
|
|
|
XR_242849.3:n.136+166A>G
|
|
|
XR_428874.2:n.136+166A>G
|
|
|
XR_930992.1:n.136+166A>G
|
|
|
XR_930994.1:n.136+166A>G
|
|
|
XR_930995.1:n.136+166A>G
|
|
|
XR_930996.1:n.136+166A>G
|
|
|
XR_930997.1:n.720+1643A>G
|
|
|
XR_930998.1:n.136+166A>G
|
|
|
XR_930999.1:n.136+166A>G
|
|
|
XR_001748105.2:n.155+166A>G
|
|
|
XR_001748106.1:n.308+166A>G
|
|
|
XR_001748108.2:n.155+166A>G
|
|
|
XR_001748109.2:n.164+166A>G
|
|
|
XR_242848.4:n.557+166A>G
|
|
|
XR_930992.3:n.155+166A>G
|
|
|
XR_930994.3:n.155+166A>G
|
|
|
XR_930995.3:n.155+166A>G
|
|
|
XR_930998.3:n.155+166A>G
|
|
|
NM_145040.3:c.384+230T>C
MANE Select
|
NP_659477.2:n.384+230T>C
|
|