ENST00000360525.9:c.352G=
MANE Select
|
ENSP00000353719.3:p.Glu118=
|
|
ENST00000329667.7:n.301G=
|
|
|
ENST00000360525.8:c.352G=
|
ENSP00000353719.3:p.Glu118=
|
|
ENST00000399098.5:c.274G=
|
ENSP00000382049.1:p.Glu92=
|
|
ENST00000399102.5:c.352G=
|
ENSP00000382053.1:p.Glu118=
|
|
ENST00000399103.5:c.352G=
|
ENSP00000382054.1:p.Glu118=
|
|
ENST00000464265.5:c.424G=
|
ENSP00000420037.1:p.Glu142=
|
|
NM_153681.2:c.424G=
|
NP_710148.1:p.Glu142=
|
|
NM_153682.2:c.352G=
|
NP_710149.1:p.Glu118=
|
|
NR_028352.1:n.699G=
|
|
|
XM_005260990.3:c.352G=
|
XP_005261047.1:p.Glu118=
|
|
XM_011529595.1:c.352G=
|
XP_011527897.1:p.Glu118=
|
|
XM_011529596.1:c.352G=
|
XP_011527898.1:p.Glu118=
|
|
NM_001320480.1:c.352G=
|
NP_001307409.1:p.Glu118=
|
|
NM_016430.3:c.274G=
|
NP_057514.2:p.Glu92=
|
|
XM_017028365.1:c.274G=
|
XP_016883854.1:p.Glu92=
|
|
NM_001320480.2:c.352G=
|
NP_001307409.1:p.Glu118=
|
|
NM_016430.4:c.274G=
|
NP_057514.2:p.Glu92=
|
|
NM_153682.3:c.352G=
MANE Select
|
NP_710149.1:p.Glu118=
|
|