ENST00000389048.8:c.3472G=
MANE Select
|
ENSP00000373700.3:p.Glu1158=
|
|
ENST00000431873.6:c.699G=
|
|
|
ENST00000638605.1:n.349G=
|
|
|
ENST00000642122.1:c.268G=
|
ENSP00000493203.1:p.Glu90=
|
|
ENST00000389048.7:c.3472G=
|
ENSP00000373700.3:p.Glu1158=
|
|
ENST00000431873.5:c.352G=
|
ENSP00000414027.2:p.Glu118=
|
|
ENST00000453137.1:c.166G=
|
ENSP00000387488.1:p.Glu56=
|
|
ENST00000618119.4:c.2341G=
|
ENSP00000482733.1:p.Glu781=
|
|
NM_004304.4:c.3472G=
|
NP_004295.2:p.Glu1158=
|
|
NM_001353765.1:c.268G=
|
NP_001340694.1:p.Glu90=
|
|
XM_024452778.1:c.625G=
|
XP_024308546.1:p.Glu209=
|
|
XM_024452779.1:c.268G=
|
XP_024308547.1:p.Glu90=
|
|
NM_004304.5:c.3472G=
MANE Select
|
NP_004295.2:p.Glu1158=
|
|
NM_001353765.2:c.268G=
|
NP_001340694.1:p.Glu90=
|
|