ENST00000317961.9:c.3689T>G
MANE Select
|
ENSP00000322408.4:p.Leu1230Arg
|
|
ENST00000317961.8:c.3689T>G
|
ENSP00000322408.4:p.Leu1230Arg
|
|
ENST00000382806.6:c.3518T>G
|
ENSP00000372256.2:p.Leu1173Arg
|
|
ENST00000415360.1:c.605T>G
|
ENSP00000389433.1:p.Leu202Arg
|
|
ENST00000440077.5:c.3566T>G
|
ENSP00000398543.1:p.Leu1189Arg
|
|
ENST00000469599.6:n.2287T>G
|
|
|
ENST00000492117.1:n.3581T>G
|
|
|
ENST00000541639.5:c.3782T>G
|
ENSP00000444293.1:p.Leu1261Arg
|
|
NM_001146705.1:c.3782T>G
|
NP_001140177.1:p.Leu1261Arg
|
|
NM_001146706.1:c.3518T>G
|
NP_001140178.1:p.Leu1173Arg
|
|
NM_004653.4:c.3689T>G
|
NP_004644.2:p.Leu1230Arg
|
|
XM_005262560.1:c.3554T>G
|
XP_005262617.1:p.Leu1185Arg
|
|
XM_005262561.1:c.3458T>G
|
XP_005262618.1:p.Leu1153Arg
|
|
XM_011531468.1:c.3611T>G
|
XP_011529770.1:p.Leu1204Arg
|
|
XR_244571.2:n.3977T>G
|
|
|
XR_430568.2:n.4311T>G
|
|
|
XM_005262560.3:c.3554T>G
|
XP_005262617.1:p.Leu1185Arg
|
|
XM_005262561.3:c.3458T>G
|
XP_005262618.1:p.Leu1153Arg
|
|
XM_011531468.3:c.3611T>G
|
XP_011529770.1:p.Leu1204Arg
|
|
XM_024452495.1:c.1679T>G
|
XP_024308263.1:p.Leu560Arg
|
|
XM_024452496.1:c.1445T>G
|
XP_024308264.1:p.Leu482Arg
|
|
XR_001756009.2:n.4427T>G
|
|
|
XR_001756010.2:n.4427T>G
|
|
|
XR_001756011.2:n.4292T>G
|
|
|
XR_001756012.2:n.4440T>G
|
|
|
XR_001756013.2:n.3758T>G
|
|
|
XR_002958832.1:n.3859T>G
|
|
|
XR_002958834.1:n.4083T>G
|
|
|
XR_002958835.1:n.3966T>G
|
|
|
XR_002958836.1:n.4649T>G
|
|
|
XR_002958837.1:n.4456T>G
|
|
|
XR_244571.4:n.3976T>G
|
|
|
XR_430568.4:n.4310T>G
|
|
|
NM_001146706.2:c.3518T>G
|
NP_001140178.1:p.Leu1173Arg
|
|
NM_004653.5:c.3689T>G
MANE Select
|
NP_004644.2:p.Leu1230Arg
|
|
NM_001146705.2:c.3782T>G
|
NP_001140177.1:p.Leu1261Arg
|
|