ENST00000454220.7:c.768G>A
|
ENSP00000391905.3:p.Glu256=
|
|
ENST00000703395.1:c.111G>A
|
ENSP00000515286.1:p.Glu37=
|
|
ENST00000703396.1:n.592G>A
|
|
|
ENST00000703397.1:c.111G>A
|
ENSP00000515287.1:p.Glu37=
|
|
ENST00000703398.1:c.690G>A
|
ENSP00000515288.1:p.Glu230=
|
|
ENST00000703421.1:n.801G>A
|
|
|
ENST00000703422.1:c.624G>A
|
ENSP00000515292.1:p.Glu208=
|
|
ENST00000703423.1:c.111G>A
|
ENSP00000515293.1:p.Glu37=
|
|
ENST00000322088.11:c.648G>A
MANE Select
|
ENSP00000324804.6:p.Glu216=
|
|
ENST00000322088.10:c.648G>A
|
ENSP00000324804.6:p.Glu216=
|
|
ENST00000454220.6:c.768G>A
|
ENSP00000391905.2:p.Glu256=
|
|
ENST00000462047.1:n.339G>A
|
|
|
ENST00000462990.5:c.111G>A
|
ENSP00000470504.1:p.Glu37=
|
|
ENST00000473820.1:n.1G>A
|
|
|
NM_014225.5:c.648G>A
|
NP_055040.2:p.Glu216=
|
|
NR_033500.1:n.842G>A
|
|
|
NM_001363656.1:c.111G>A
|
NP_001350585.1:p.Glu37=
|
|
NM_014225.6:c.648G>A
MANE Select
|
NP_055040.2:p.Glu216=
|
|
NM_001363656.2:c.111G>A
|
NP_001350585.1:p.Glu37=
|
|
NR_033500.2:n.592G>A
|
|
|