ENST00000333371.8:c.-214G>A
MANE Select
|
ENSP00000327650.4:n.-214G>A
|
|
ENST00000643536.1:c.-214G>A
|
ENSP00000494429.1:n.-214G>A
|
|
ENST00000333371.7:c.-214G>A
|
ENSP00000327650.3:n.-214G>A
|
|
ENST00000535906.1:c.-214G>A
|
ENSP00000444053.1:n.-214G>A
|
|
ENST00000556096.6:n.141G>A
|
|
|
ENST00000557358.1:n.134G>A
|
|
|
ENST00000574755.5:c.-214G>A
|
ENSP00000460413.1:n.-214G>A
|
|
NM_001289148.1:c.-214G>A
|
NP_001276077.1:n.-214G>A
|
|
NM_001289149.1:c.-425G>A
|
NP_001276078.1:n.-425G>A
|
|
NM_018668.4:c.-214G>A , LRG_884t1:c.-214G>A
|
NP_061138.3:n.-214G>A
|
|
XM_005254884.2:c.-214G>A
|
XP_005254941.1:n.-214G>A
|
|
XM_005254887.1:c.-344G>A
|
XP_005254944.1:n.-344G>A
|
|
XM_005254888.2:c.-214G>A
|
XP_005254945.1:n.-214G>A
|
|
XM_011521448.1:c.-527G>A
|
XP_011519750.1:n.-527G>A
|
|
XM_017022075.2:c.-575G>A
|
XP_016877564.1:n.-575G>A
|
|
XM_017022076.1:c.-432G>A
|
XP_016877565.1:n.-432G>A
|
|
XR_001751213.2:n.123G>A
|
|
|
NM_018668.5:c.-214G>A
MANE Select
|
NP_061138.3:n.-214G>A
|
|