ENST00000374762.4:c.430+654C>T
MANE Select
|
ENSP00000363894.3:n.430+654C>T
|
|
ENST00000374762.3:c.430+654C>T
|
ENSP00000363894.3:n.430+654C>T
|
|
ENST00000460936.5:c.430+654C>T
|
ENSP00000435209.1:n.430+654C>T
|
|
ENST00000461177.1:n.265+654C>T
|
|
|
NM_018376.3:c.430+654C>T
|
NP_060846.2:n.430+654C>T
|
|
NR_130759.1:n.719+654C>T
|
|
|
NR_130760.1:n.930+654C>T
|
|
|
XM_011518839.1:c.430+654C>T
|
XP_011517141.1:n.430+654C>T
|
|
XR_428532.1:n.930+654C>T
|
|
|
XR_001746344.1:n.930+654C>T
|
|
|
XR_001746345.1:n.930+654C>T
|
|
|
NM_018376.4:c.430+654C>T
MANE Select
|
NP_060846.2:n.430+654C>T
|
|
NR_130759.2:n.331+654C>T
|
|
|
NR_130760.2:n.542+654C>T
|
|
|