|
ENST00000394867.9:n.1717G=
|
|
|
|
ENST00000688002.1:n.3429G=
|
|
|
|
ENST00000688751.1:n.414G=
|
|
|
|
ENST00000689792.1:n.1182G=
|
|
|
|
ENST00000262948.10:c.*75G=
MANE Select
|
ENSP00000262948.4:n.*75G=
|
|
|
ENST00000262948.9:c.*75G=
|
ENSP00000262948.3:n.*75G=
|
|
|
ENST00000394867.8:c.*75G=
|
ENSP00000378336.1:n.*75G=
|
|
|
ENST00000597263.5:n.463G=
|
|
|
|
ENST00000600584.5:n.2727G=
|
|
|
|
ENST00000601786.5:n.1579G=
|
|
|
|
NM_030662.3:c.*75G= , LRG_750t1:c.*75G=
|
NP_109587.1:n.*75G=
|
|
|
XM_006722799.2:c.*75G=
|
XP_006722862.1:n.*75G=
|
|
|
XM_011528133.1:c.*75G=
|
XP_011526435.1:n.*75G=
|
|
|
NM_030662.4:c.*75G=
MANE Select
|
NP_109587.1:n.*75G=
|
|
