ENST00000375731.9:c.704A>T
MANE Select
|
ENSP00000364883.5:p.Glu235Val
|
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ENST00000303617.5:c.617A>T
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ENSP00000307334.5:p.Glu206Val
|
|
ENST00000375731.8:c.704A>T
|
ENSP00000364883.4:p.Glu235Val
|
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NM_001306190.1:c.617A>T
|
NP_001293119.1:p.Glu206Val
|
|
NM_001698.2:c.704A>T , LRG_449t1:c.704A>T
|
NP_001689.1:p.Glu235Val
|
|
XM_005252066.2:c.734A>T
|
XP_005252123.1:p.Glu245Val
|
|
XM_005252067.3:c.734A>T
|
XP_005252124.1:p.Glu245Val
|
|
XM_005252069.3:c.734A>T
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XP_005252126.1:p.Glu245Val
|
|
XM_005252073.2:c.242A>T
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XP_005252130.1:p.Glu81Val
|
|
XM_006717150.2:c.647A>T
|
XP_006717213.1:p.Glu216Val
|
|
XM_011518801.1:c.380A>T
|
XP_011517103.1:p.Glu127Val
|
|
XM_011518802.1:c.377A>T
|
XP_011517104.1:p.Glu126Val
|
|
NM_001351431.1:c.377A>T
|
NP_001338360.1:p.Glu126Val
|
|
NM_001351432.1:c.377A>T
|
NP_001338361.1:p.Glu126Val
|
|
NM_001351433.1:c.377A>T
|
NP_001338362.1:p.Glu126Val
|
|
XM_005252066.3:c.734A>T
|
XP_005252123.1:p.Glu245Val
|
|
XM_005252067.4:c.734A>T
|
XP_005252124.1:p.Glu245Val
|
|
XM_005252069.4:c.734A>T
|
XP_005252126.1:p.Glu245Val
|
|
XM_006717150.3:c.647A>T
|
XP_006717213.1:p.Glu216Val
|
|
XM_017014849.1:c.704A>T
|
XP_016870338.1:p.Glu235Val
|
|
XR_001746328.2:n.929A>T
|
|
|
XR_001746329.2:n.881A>T
|
|
|
NM_001698.3:c.704A>T
MANE Select
|
NP_001689.1:p.Glu235Val
|
|
NM_001306190.2:c.617A>T
|
NP_001293119.1:p.Glu206Val
|
|
NM_001351431.2:c.377A>T
|
NP_001338360.1:p.Glu126Val
|
|
NM_001351432.2:c.377A>T
|
NP_001338361.1:p.Glu126Val
|
|
NM_001351433.2:c.377A>T
|
NP_001338362.1:p.Glu126Val
|
|