ENST00000437033.7:c.237A>G
MANE Select
|
ENSP00000414254.2:p.Glu79=
|
|
ENST00000209665.8:c.273A>G
|
ENSP00000209665.4:p.Glu91=
|
|
ENST00000437033.6:c.237A>G
|
ENSP00000414254.2:p.Glu79=
|
|
ENST00000474027.1:c.66A>G
|
ENSP00000420300.1:p.Glu22=
|
|
ENST00000476959.5:c.297A>G
|
ENSP00000420269.1:p.Glu99=
|
|
ENST00000482593.5:c.66A>G
|
ENSP00000420613.1:p.Glu22=
|
|
NM_000673.4:c.273A>G
|
NP_000664.2:p.Glu91=
|
|
NM_001166504.1:c.297A>G
|
NP_001159976.1:p.Glu99=
|
|
NM_000673.7:c.237A>G
MANE Select
|
NP_000664.3:p.Glu79=
|
|
NM_001166504.2:c.297A>G
|
NP_001159976.1:p.Glu99=
|
|