ENST00000324071.10:c.987A>G
MANE Select
|
ENSP00000324648.2:p.Glu329=
|
|
ENST00000598834.2:c.1011A>G
|
|
|
ENST00000324071.8:c.987A>G
|
ENSP00000324648.2:p.Glu329=
|
|
ENST00000593831.1:c.279A>G
|
ENSP00000470582.1:p.Glu93=
|
|
ENST00000597612.1:n.482A>G
|
|
|
NM_000767.4:c.987A>G
|
NP_000758.1:p.Glu329=
|
|
XM_005258569.3:c.987A>G
|
XP_005258626.1:p.Glu329=
|
|
XM_006723050.2:c.987A>G
|
XP_006723113.1:p.Glu329=
|
|
XM_011526546.1:c.987A>G
|
XP_011524848.1:p.Glu329=
|
|
XM_011526547.1:c.987A>G
|
XP_011524849.1:p.Glu329=
|
|
XM_011526548.1:c.507A>G
|
XP_011524850.1:p.Glu169=
|
|
XM_011526549.1:c.396A>G
|
XP_011524851.1:p.Glu132=
|
|
XM_011526550.1:c.387A>G
|
XP_011524852.1:p.Glu129=
|
|
NM_000767.5:c.987A>G
MANE Select
|
NP_000758.1:p.Glu329=
|
|