ENST00000333371.8:c.-176G>A
MANE Select
|
ENSP00000327650.4:n.-176G>A
|
|
ENST00000643536.1:c.-176G>A
|
ENSP00000494429.1:n.-176G>A
|
|
ENST00000333371.7:c.-176G>A
|
ENSP00000327650.3:n.-176G>A
|
|
ENST00000535906.1:c.-176G>A
|
ENSP00000444053.1:n.-176G>A
|
|
ENST00000556096.6:n.179G>A
|
|
|
ENST00000557358.1:n.172G>A
|
|
|
ENST00000574755.5:c.-176G>A
|
ENSP00000460413.1:n.-176G>A
|
|
NM_001289148.1:c.-176G>A
|
NP_001276077.1:n.-176G>A
|
|
NM_001289149.1:c.-387G>A
|
NP_001276078.1:n.-387G>A
|
|
NM_018668.4:c.-176G>A , LRG_884t1:c.-176G>A
|
NP_061138.3:n.-176G>A
|
|
XM_005254884.2:c.-176G>A
|
XP_005254941.1:n.-176G>A
|
|
XM_005254887.1:c.-306G>A
|
XP_005254944.1:n.-306G>A
|
|
XM_005254888.2:c.-176G>A
|
XP_005254945.1:n.-176G>A
|
|
XM_011521448.1:c.-489G>A
|
XP_011519750.1:n.-489G>A
|
|
XM_017022075.2:c.-537G>A
|
XP_016877564.1:n.-537G>A
|
|
XM_017022076.1:c.-394G>A
|
XP_016877565.1:n.-394G>A
|
|
XR_001751213.2:n.161G>A
|
|
|
NM_018668.5:c.-176G>A
MANE Select
|
NP_061138.3:n.-176G>A
|
|