ENST00000265724.8:c.2928-162G=
|
ENSP00000265724.3:n.2928-162G=
|
|
ENST00000622132.5:c.2928-162G=
MANE Select
|
ENSP00000478255.1:n.2928-162G=
|
|
ENST00000265724.7:c.2928-162G=
|
ENSP00000265724.3:n.2928-162G=
|
|
ENST00000475929.5:n.84-162G=
|
|
|
ENST00000483831.1:n.486-162G=
|
|
|
ENST00000488737.6:n.570-162G=
|
|
|
ENST00000496821.5:n.556-162G=
|
|
|
ENST00000543898.5:c.2736-162G=
|
ENSP00000444095.1:n.2736-162G=
|
|
ENST00000622132.4:c.2928-162G=
|
ENSP00000478255.1:n.2928-162G=
|
|
NM_000927.4:c.2928-162G=
|
NP_000918.2:n.2928-162G=
|
|
NM_001348944.1:c.2928-162G=
|
NP_001335873.1:n.2928-162G=
|
|
NM_001348945.1:c.3138-162G=
|
NP_001335874.1:n.3138-162G=
|
|
NM_001348946.1:c.2928-162G=
|
NP_001335875.1:n.2928-162G=
|
|
NM_001348946.2:c.2928-162G=
MANE Select
|
NP_001335875.1:n.2928-162G=
|
|
NM_000927.5:c.2928-162G=
|
NP_000918.2:n.2928-162G=
|
|
NM_001348944.2:c.2928-162G=
|
NP_001335873.1:n.2928-162G=
|
|
NM_001348945.2:c.3138-162G=
|
NP_001335874.1:n.3138-162G=
|
|