NM_001551.3:c.871+212T>G
MANE Select
|
NP_001542.1:n.871+212T>G
|
ENST00000356413.5:c.871+212T>G
MANE Select
|
ENSP00000348784.4:n.871+212T>G
|
NM_001370192.1:c.871+212T>G
|
NP_001357121.1:n.871+212T>G
|
NM_001370193.1:c.871+212T>G
|
NP_001357122.1:n.871+212T>G
|
NM_001370194.1:c.595+212T>G
|
NP_001357123.1:n.595+212T>G
|
NM_001551.2:c.871+212T>G
|
NP_001542.1:n.871+212T>G
|
ENST00000342206.10:c.871+212T>G
|
ENSP00000363661.5:n.871+212T>G
|
ENST00000356413.4:c.871+212T>G
|
ENSP00000348784.4:n.871+212T>G
|
XM_017029489.1:c.871+212T>G
|
XP_016884978.1:n.871+212T>G
|
XR_002958775.1:n.1174+212T>G
|
|
XR_938398.1:n.1370+212T>G
|
|
XR_938399.1:n.1174+212T>G
|
|