ENST00000261884.8:c.1044-134G>A
MANE Select
|
ENSP00000261884.3:n.1044-134G>A
|
|
ENST00000261884.7:c.1044-134G>A
|
ENSP00000261884.3:n.1044-134G>A
|
|
ENST00000560475.1:c.111+4123G>A
|
|
|
ENST00000560567.5:c.1043+4123G>A
|
ENSP00000453106.1:n.1043+4123G>A
|
|
NM_016213.4:c.1044-134G>A
|
NP_057297.2:n.1044-134G>A
|
|
XM_005254789.1:c.354-134G>A
|
XP_005254846.1:n.354-134G>A
|
|
XR_243130.1:n.1101+4123G>A
|
|
|
NM_001321924.1:c.354-134G>A
|
NP_001308853.1:n.354-134G>A
|
|
NR_135855.1:n.1103+4123G>A
|
|
|
NM_001321924.2:c.354-134G>A
|
NP_001308853.1:n.354-134G>A
|
|
NM_016213.5:c.1044-134G>A
MANE Select
|
NP_057297.2:n.1044-134G>A
|
|
NR_135855.2:n.1071+4123G>A
|
|
|