ENST00000261799.9:c.2586+51A>G
MANE Select
|
ENSP00000261799.4:n.2586+51A>G
|
|
ENST00000261799.8:c.2586+51A>G
|
ENSP00000261799.4:n.2586+51A>G
|
|
ENST00000519575.5:n.500+51A>G
|
|
|
ENST00000520579.5:c.*1900+51A>G
|
ENSP00000430026.1:n.*1900+51A>G
|
|
NM_002609.3:c.2586+51A>G
|
NP_002600.1:n.2586+51A>G
|
|
XM_005268464.2:c.2394+51A>G
|
XP_005268521.1:n.2394+51A>G
|
|
XM_011537658.1:c.2586+51A>G
|
XP_011535960.1:n.2586+51A>G
|
|
XM_011537659.1:c.2586+51A>G
|
XP_011535961.1:n.2586+51A>G
|
|
XM_011537660.1:c.2586+51A>G
|
XP_011535962.1:n.2586+51A>G
|
|
NM_001355016.1:c.2394+51A>G
|
NP_001341945.1:n.2394+51A>G
|
|
NM_001355017.1:c.2103+51A>G
|
NP_001341946.1:n.2103+51A>G
|
|
NM_002609.4:c.2586+51A>G
MANE Select
|
NP_002600.1:n.2586+51A>G
|
|
NM_001355016.2:c.2394+51A>G
|
NP_001341945.1:n.2394+51A>G
|
|
NM_001355017.2:c.2103+51A>G
|
NP_001341946.1:n.2103+51A>G
|
|