ENST00000394867.9:n.1836T>A
|
|
|
ENST00000688751.1:n.533T>A
|
|
|
ENST00000689792.1:n.1301T>A
|
|
|
ENST00000262948.10:c.*194T>A
MANE Select
|
ENSP00000262948.4:n.*194T>A
|
|
ENST00000262948.9:c.*194T>A
|
ENSP00000262948.3:n.*194T>A
|
|
ENST00000394867.8:c.*194T>A
|
ENSP00000378336.1:n.*194T>A
|
|
ENST00000600584.5:n.2846T>A
|
|
|
ENST00000601786.5:n.1698T>A
|
|
|
NM_030662.3:c.*194T>A , LRG_750t1:c.*194T>A
|
NP_109587.1:n.*194T>A
|
|
XM_006722799.2:c.*194T>A
|
XP_006722862.1:n.*194T>A
|
|
XM_011528133.1:c.*194T>A
|
XP_011526435.1:n.*194T>A
|
|
NM_030662.4:c.*194T>A
MANE Select
|
NP_109587.1:n.*194T>A
|
|