ENST00000322048.12:c.406T>A
MANE Select
|
ENSP00000322832.6:p.Phe136Ile
|
|
ENST00000322048.11:c.406T>A
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ENSP00000322832.5:p.Phe136Ile
|
|
ENST00000585653.1:n.538T>A
|
|
|
ENST00000586153.1:c.151T>A
|
ENSP00000464699.1:p.Phe51Ile
|
|
ENST00000586336.5:n.505T>A
|
|
|
ENST00000586504.5:c.186T>A
|
|
|
ENST00000587377.5:c.406T>A
|
ENSP00000468343.1:p.Phe136Ile
|
|
ENST00000587711.5:c.118-1045T>A
|
ENSP00000467459.1:n.118-1045T>A
|
|
ENST00000587843.5:c.*144T>A
|
ENSP00000465970.1:n.*144T>A
|
|
ENST00000588201.5:c.*263T>A
|
ENSP00000466529.1:n.*263T>A
|
|
ENST00000589543.5:n.363T>A
|
|
|
ENST00000591292.5:n.1735T>A
|
|
|
ENST00000591392.5:c.334T>A
|
ENSP00000467509.1:p.Phe112Ile
|
|
ENST00000592019.1:c.76+49T>A
|
|
|
NM_024589.2:c.406T>A , LRG_455t1:c.406T>A
|
NP_078865.1:p.Phe136Ile
|
|
NR_046480.1:n.730T>A
|
|
|
XM_006720947.2:c.406T>A
|
XP_006721010.1:p.Phe136Ile
|
|
XM_006720948.2:c.136T>A
|
XP_006721011.1:p.Phe46Ile
|
|
XM_006720947.4:c.406T>A
|
XP_006721010.1:p.Phe136Ile
|
|
XM_006720948.4:c.136T>A
|
XP_006721011.1:p.Phe46Ile
|
|
NM_024589.3:c.406T>A
MANE Select
|
NP_078865.1:p.Phe136Ile
|
|
NR_046480.2:n.413T>A
|
|
|