ENST00000333371.8:c.1656A>T
MANE Select
|
ENSP00000327650.4:p.Thr552=
|
|
ENST00000643536.1:c.1656A>T
|
ENSP00000494429.1:p.Thr552=
|
|
ENST00000647331.1:c.1656A>T
|
ENSP00000493953.1:p.Thr552=
|
|
ENST00000333371.7:c.1656A>T
|
ENSP00000327650.3:p.Thr552=
|
|
ENST00000535906.1:c.1575A>T
|
ENSP00000444053.1:p.Thr525=
|
|
ENST00000554660.1:n.591A>T
|
|
|
ENST00000557470.5:n.147+589A>T
|
|
|
ENST00000574755.5:c.*1351A>T
|
ENSP00000460413.1:n.*1351A>T
|
|
NM_001289148.1:c.1575A>T
|
NP_001276077.1:p.Thr525=
|
|
NM_001289149.1:c.1383A>T
|
NP_001276078.1:p.Thr461=
|
|
NM_018668.4:c.1656A>T , LRG_884t1:c.1656A>T
|
NP_061138.3:p.Thr552=
|
|
XM_005254884.2:c.1578A>T
|
XP_005254941.1:p.Thr526=
|
|
XM_005254887.1:c.1383A>T
|
XP_005254944.1:p.Thr461=
|
|
XM_011521448.1:c.1383A>T
|
XP_011519750.1:p.Thr461=
|
|
XM_011521449.1:c.1332A>T
|
XP_011519751.1:p.Thr444=
|
|
XM_011521449.2:c.1332A>T
|
XP_011519751.1:p.Thr444=
|
|
XM_017022075.2:c.1311A>T
|
XP_016877564.1:p.Thr437=
|
|
XM_017022076.1:c.1311A>T
|
XP_016877565.1:p.Thr437=
|
|
XR_001751213.2:n.2154A>T
|
|
|
NM_018668.5:c.1656A>T
MANE Select
|
NP_061138.3:p.Thr552=
|
|