ENST00000369538.4:c.1213-1G=
|
ENSP00000358551.4:n.1213-1G=
|
|
ENST00000520113.7:c.1225-1G=
MANE Select
|
ENSP00000430075.3:n.1225-1G=
|
|
ENST00000637080.1:c.1008-1G=
|
ENSP00000489753.1:n.1008-1G=
|
|
ENST00000639077.1:n.890-1G=
|
|
|
ENST00000369538.3:c.1312-1G=
|
ENSP00000358551.3:n.1312-1G=
|
|
ENST00000520113.6:c.1324-1G=
|
ENSP00000430075.2:n.1324-1G=
|
|
NM_000036.2:c.1324-1G=
|
NP_000027.2:n.1324-1G=
|
|
NM_001172626.1:c.1312-1G=
|
NP_001166097.1:n.1312-1G=
|
|
NM_000036.3:c.1225-1G=
MANE Select
|
NP_000027.3:n.1225-1G=
|
|
NM_001172626.2:c.1213-1G=
|
NP_001166097.2:n.1213-1G=
|
|