ENST00000706952.1:c.3151T>G
|
ENSP00000516672.1:p.Phe1051Val
|
|
ENST00000638521.1:c.944T>G
|
|
|
ENST00000638869.1:c.453T>G
|
|
|
ENST00000639642.1:c.282T>G
|
|
|
ENST00000640005.1:c.55T>G
|
ENSP00000491293.1:p.Phe19Val
|
|
ENST00000640694.1:c.2992T>G
|
ENSP00000492403.1:p.Phe998Val
|
|
ENST00000642864.1:c.2992T>G
MANE Select
|
ENSP00000495726.1:p.Phe998Val
|
|
ENST00000674510.1:c.2992T>G
|
ENSP00000502054.1:p.Phe998Val
|
|
ENST00000674761.1:n.1299T>G
|
|
|
ENST00000675719.1:c.2962T>G
|
ENSP00000501927.1:p.Phe988Val
|
|
ENST00000375365.2:c.2377T>G
|
ENSP00000364514.2:p.Phe793Val
|
|
ENST00000396435.7:c.2992T>G
|
ENSP00000379712.3:p.Phe998Val
|
|
NM_001111125.2:c.2992T>G
|
NP_001104595.1:p.Phe998Val
|
|
NM_015075.1:c.2377T>G
|
NP_055890.1:p.Phe793Val
|
|
XM_006724579.2:c.3088T>G
|
XP_006724642.1:p.Phe1030Val
|
|
XM_006724580.2:c.2377T>G
|
XP_006724643.1:p.Phe793Val
|
|
XM_006724581.2:c.3088T>G
|
XP_006724644.1:p.Phe1030Val
|
|
XM_006724582.2:c.3088T>G
|
XP_006724645.1:p.Phe1030Val
|
|
XM_006724583.2:c.3088T>G
|
XP_006724646.1:p.Phe1030Val
|
|
XM_006724584.2:c.3088T>G
|
XP_006724647.1:p.Phe1030Val
|
|
XM_011530772.1:c.2314T>G
|
XP_011529074.1:p.Phe772Val
|
|
XM_011530773.1:c.2281T>G
|
XP_011529075.1:p.Phe761Val
|
|
XM_011530774.1:c.3088T>G
|
XP_011529076.1:p.Phe1030Val
|
|
XM_011530775.1:c.3088T>G
|
XP_011529077.1:p.Phe1030Val
|
|
XM_011530776.1:c.3088T>G
|
XP_011529078.1:p.Phe1030Val
|
|
XM_011530777.1:c.3088T>G
|
XP_011529079.1:p.Phe1030Val
|
|
XR_938365.1:n.3315T>G
|
|
|
XM_006724579.3:c.3088T>G
|
XP_006724642.1:p.Phe1030Val
|
|
XM_006724580.3:c.2377T>G
|
XP_006724643.1:p.Phe793Val
|
|
XM_006724581.4:c.3088T>G
|
XP_006724644.1:p.Phe1030Val
|
|
XM_006724582.4:c.3088T>G
|
XP_006724645.1:p.Phe1030Val
|
|
XM_006724583.4:c.3088T>G
|
XP_006724646.1:p.Phe1030Val
|
|
XM_006724584.3:c.3088T>G
|
XP_006724647.1:p.Phe1030Val
|
|
XM_011530773.2:c.2281T>G
|
XP_011529075.1:p.Phe761Val
|
|
XM_011530774.3:c.3088T>G
|
XP_011529076.1:p.Phe1030Val
|
|
XM_011530776.2:c.3088T>G
|
XP_011529078.1:p.Phe1030Val
|
|
XM_011530777.2:c.3088T>G
|
XP_011529079.1:p.Phe1030Val
|
|
XM_017029359.2:c.2962T>G
|
XP_016884848.1:p.Phe988Val
|
|
XM_017029360.1:c.2494T>G
|
XP_016884849.1:p.Phe832Val
|
|
XR_938365.2:n.3309T>G
|
|
|
NM_001111125.3:c.2992T>G
MANE Select
|
NP_001104595.1:p.Phe998Val
|
|
NM_015075.2:c.2377T>G
|
NP_055890.1:p.Phe793Val
|
|