ENST00000333371.8:c.-223G>T
MANE Select
|
ENSP00000327650.4:n.-223G>T
|
|
ENST00000643536.1:c.-223G>T
|
ENSP00000494429.1:n.-223G>T
|
|
ENST00000333371.7:c.-223G>T
|
ENSP00000327650.3:n.-223G>T
|
|
ENST00000535906.1:c.-223G>T
|
ENSP00000444053.1:n.-223G>T
|
|
ENST00000556096.6:n.132G>T
|
|
|
ENST00000557358.1:n.125G>T
|
|
|
ENST00000574755.5:c.-223G>T
|
ENSP00000460413.1:n.-223G>T
|
|
NM_001289148.1:c.-223G>T
|
NP_001276077.1:n.-223G>T
|
|
NM_001289149.1:c.-434G>T
|
NP_001276078.1:n.-434G>T
|
|
NM_018668.4:c.-223G>T , LRG_884t1:c.-223G>T
|
NP_061138.3:n.-223G>T
|
|
XM_005254884.2:c.-223G>T
|
XP_005254941.1:n.-223G>T
|
|
XM_005254887.1:c.-353G>T
|
XP_005254944.1:n.-353G>T
|
|
XM_005254888.2:c.-223G>T
|
XP_005254945.1:n.-223G>T
|
|
XM_011521448.1:c.-536G>T
|
XP_011519750.1:n.-536G>T
|
|
XM_017022075.2:c.-584G>T
|
XP_016877564.1:n.-584G>T
|
|
XM_017022076.1:c.-441G>T
|
XP_016877565.1:n.-441G>T
|
|
XR_001751213.2:n.114G>T
|
|
|
NM_018668.5:c.-223G>T
MANE Select
|
NP_061138.3:n.-223G>T
|
|