ENST00000392668.8:c.69+6004G>A
MANE Select
|
ENSP00000376436.3:n.69+6004G>A
|
|
ENST00000525404.5:n.138+6004G>A
|
|
|
NM_001143820.1:c.69+6004G>A
|
NP_001137292.1:n.69+6004G>A
|
|
XM_011542649.1:c.69+6004G>A
|
XP_011540951.1:n.69+6004G>A
|
|
XM_011542651.1:c.69+6004G>A
|
XP_011540953.1:n.69+6004G>A
|
|
XR_948162.1:n.749+602C>T
|
|
|
XR_948163.1:n.749+602C>T
|
|
|
XM_017017314.1:c.69+6004G>A
|
XP_016872803.1:n.69+6004G>A
|
|
XM_017017315.2:c.-36-10623G>A
|
XP_016872804.1:n.-36-10623G>A
|
|
XM_017017317.1:c.69+6004G>A
|
XP_016872806.1:n.69+6004G>A
|
|
XR_948162.2:n.953+602C>T
|
|
|
XR_948163.2:n.953+602C>T
|
|
|
NM_001143820.2:c.69+6004G>A
MANE Select
|
NP_001137292.1:n.69+6004G>A
|
|