|
ENST00000394867.9:n.1780A=
|
|
|
|
ENST00000688751.1:n.477A=
|
|
|
|
ENST00000689792.1:n.1245A=
|
|
|
|
ENST00000262948.10:c.*138A=
MANE Select
|
ENSP00000262948.4:n.*138A=
|
|
|
ENST00000262948.9:c.*138A=
|
ENSP00000262948.3:n.*138A=
|
|
|
ENST00000394867.8:c.*138A=
|
ENSP00000378336.1:n.*138A=
|
|
|
ENST00000597263.5:n.526A=
|
|
|
|
ENST00000600584.5:n.2790A=
|
|
|
|
ENST00000601786.5:n.1642A=
|
|
|
|
NM_030662.3:c.*138A= , LRG_750t1:c.*138A=
|
NP_109587.1:n.*138A=
|
|
|
XM_006722799.2:c.*138A=
|
XP_006722862.1:n.*138A=
|
|
|
XM_011528133.1:c.*138A=
|
XP_011526435.1:n.*138A=
|
|
|
NM_030662.4:c.*138A=
MANE Select
|
NP_109587.1:n.*138A=
|
|
