ENST00000265724.8:c.2398-217G=
|
ENSP00000265724.3:n.2398-217G=
|
|
ENST00000622132.5:c.2398-217G=
MANE Select
|
ENSP00000478255.1:n.2398-217G=
|
|
ENST00000265724.7:c.2398-217G=
|
ENSP00000265724.3:n.2398-217G=
|
|
ENST00000496821.5:n.26-217G=
|
|
|
ENST00000543898.5:c.2206-217G=
|
ENSP00000444095.1:n.2206-217G=
|
|
ENST00000622132.4:c.2398-217G=
|
ENSP00000478255.1:n.2398-217G=
|
|
NM_000927.4:c.2398-217G=
|
NP_000918.2:n.2398-217G=
|
|
NM_001348944.1:c.2398-217G=
|
NP_001335873.1:n.2398-217G=
|
|
NM_001348945.1:c.2608-217G=
|
NP_001335874.1:n.2608-217G=
|
|
NM_001348946.1:c.2398-217G=
|
NP_001335875.1:n.2398-217G=
|
|
NM_001348946.2:c.2398-217G=
MANE Select
|
NP_001335875.1:n.2398-217G=
|
|
NM_000927.5:c.2398-217G=
|
NP_000918.2:n.2398-217G=
|
|
NM_001348944.2:c.2398-217G=
|
NP_001335873.1:n.2398-217G=
|
|
NM_001348945.2:c.2608-217G=
|
NP_001335874.1:n.2608-217G=
|
|