ENST00000380743.9:c.*4-169T>C
MANE Select
|
ENSP00000370119.4:n.*4-169T>C
|
|
ENST00000380742.8:c.*4-169T>C
|
ENSP00000370118.4:n.*4-169T>C
|
|
ENST00000380743.8:c.*4-169T>C
|
ENSP00000370119.4:n.*4-169T>C
|
|
ENST00000505346.5:n.630T>C
|
|
|
ENST00000506734.5:c.*59-169T>C
|
ENSP00000424799.1:n.*59-169T>C
|
|
ENST00000507458.2:c.143-169T>C
|
|
|
ENST00000514914.1:n.430-169T>C
|
|
|
ENST00000626847.2:c.835-169T>C
|
ENSP00000486152.1:n.835-169T>C
|
|
NM_017411.3:c.*4-169T>C
|
NP_059107.1:n.*4-169T>C
|
|
NM_022875.2:c.835-169T>C
|
NP_075013.1:n.835-169T>C
|
|
NM_022876.2:c.*4-169T>C
|
NP_075014.1:n.*4-169T>C
|
|
NM_022877.2:c.739-169T>C
|
NP_075015.1:n.739-169T>C
|
|
XM_011543600.1:c.*4-169T>C
|
XP_011541902.1:n.*4-169T>C
|
|
XM_011543601.1:c.634-169T>C
|
XP_011541903.1:n.634-169T>C
|
|
XM_011543602.1:c.*4-169T>C
|
XP_011541904.1:n.*4-169T>C
|
|
XM_011543603.1:c.538-169T>C
|
XP_011541905.1:n.538-169T>C
|
|
XR_948432.1:n.1054+88846T>C
|
|
|
XM_011543600.2:c.*4-169T>C
|
XP_011541902.1:n.*4-169T>C
|
|
XM_011543602.3:c.*4-169T>C
|
XP_011541904.1:n.*4-169T>C
|
|
XM_011543603.3:c.538-169T>C
|
XP_011541905.1:n.538-169T>C
|
|
NM_017411.4:c.*4-169T>C
MANE Select
|
NP_059107.1:n.*4-169T>C
|
|
NM_022875.3:c.835-169T>C
|
NP_075013.1:n.835-169T>C
|
|