ENST00000265724.8:c.3225G>T
|
ENSP00000265724.3:p.Gly1075=
|
|
ENST00000622132.5:c.3225G>T
MANE Select
|
ENSP00000478255.1:p.Gly1075=
|
|
ENST00000265724.7:c.3225G>T
|
ENSP00000265724.3:p.Gly1075=
|
|
ENST00000475929.5:n.381G>T
|
|
|
ENST00000488737.6:n.867G>T
|
|
|
ENST00000496821.5:n.853G>T
|
|
|
ENST00000543898.5:c.3033G>T
|
ENSP00000444095.1:p.Gly1011=
|
|
ENST00000622132.4:c.3225G>T
|
ENSP00000478255.1:p.Gly1075=
|
|
NM_000927.4:c.3225G>T
|
NP_000918.2:p.Gly1075=
|
|
NM_001348944.1:c.3225G>T
|
NP_001335873.1:p.Gly1075=
|
|
NM_001348945.1:c.3435G>T
|
NP_001335874.1:p.Gly1145=
|
|
NM_001348946.1:c.3225G>T
|
NP_001335875.1:p.Gly1075=
|
|
NM_001348946.2:c.3225G>T
MANE Select
|
NP_001335875.1:p.Gly1075=
|
|
NM_000927.5:c.3225G>T
|
NP_000918.2:p.Gly1075=
|
|
NM_001348944.2:c.3225G>T
|
NP_001335873.1:p.Gly1075=
|
|
NM_001348945.2:c.3435G>T
|
NP_001335874.1:p.Gly1145=
|
|