ENST00000261643.8:c.-41G=
MANE Select
|
ENSP00000261643.3:n.-41G=
|
|
ENST00000664217.1:c.-41G=
|
ENSP00000499396.1:n.-41G=
|
|
ENST00000670279.1:c.-41G=
|
ENSP00000499450.1:n.-41G=
|
|
ENST00000261643.7:c.-41G=
|
ENSP00000261643.3:n.-41G=
|
|
ENST00000429152.6:c.-41G=
|
ENSP00000397750.2:n.-41G=
|
|
NM_001303.3:c.-41G=
|
NP_001294.2:n.-41G=
|
|
XM_005256458.1:c.-41G=
|
XP_005256515.1:n.-41G=
|
|
XM_011523657.1:c.-41G=
|
XP_011521959.1:n.-41G=
|
|
XM_011523658.1:c.-492G=
|
XP_011521960.1:n.-492G=
|
|
XR_933974.1:n.63G=
|
|
|
XR_933975.1:n.63G=
|
|
|
NM_001303.4:c.-41G=
MANE Select
|
NP_001294.2:n.-41G=
|
|