|
ENST00000700029.2:c.912T>G
|
ENSP00000514759.2:p.Phe304Leu
|
|
|
ENST00000710265.1:c.819T>G
|
ENSP00000518161.1:p.Phe273Leu
|
|
|
ENST00000472832.3:c.819T>G
|
ENSP00000483066.2:p.Phe273Leu
|
|
|
ENST00000688158.2:n.1554T>G
|
|
|
|
ENST00000688922.2:c.*649T>G
|
ENSP00000508742.2:n.*649T>G
|
|
|
ENST00000700021.1:c.774T>G
|
ENSP00000514757.1:p.Phe258Leu
|
|
|
ENST00000700022.1:c.*158T>G
|
ENSP00000514758.1:n.*158T>G
|
|
|
ENST00000700023.1:n.1977T>G
|
|
|
|
ENST00000700024.1:n.2211T>G
|
|
|
|
ENST00000700025.1:n.1588T>G
|
|
|
|
ENST00000700026.1:n.456T>G
|
|
|
|
ENST00000700029.1:c.746T>G
|
|
|
|
ENST00000706954.1:c.819T>G
|
ENSP00000516674.1:p.Phe273Leu
|
|
|
ENST00000706955.1:c.*854T>G
|
ENSP00000516675.1:n.*854T>G
|
|
|
ENST00000686459.1:c.*405T>G
|
ENSP00000508909.1:n.*405T>G
|
|
|
ENST00000688158.1:c.*930T>G
|
ENSP00000509254.1:n.*930T>G
|
|
|
ENST00000688308.1:c.819T>G
|
ENSP00000508752.1:p.Phe273Leu
|
|
|
ENST00000688922.1:c.740T>G
|
|
|
|
ENST00000693560.1:c.1338T>G
|
ENSP00000509861.1:p.Phe446Leu
|
|
|
ENST00000371953.8:c.819T>G
MANE Select
|
ENSP00000361021.3:p.Phe273Leu
|
|
|
ENST00000371953.7:c.819T>G
|
ENSP00000361021.3:p.Phe273Leu
|
|
|
ENST00000472832.2:c.246T>G
|
ENSP00000483066.1:p.Phe82Leu
|
|
|
NM_000314.5:c.819T>G
|
NP_000305.3:p.Phe273Leu
|
|
|
NM_000314.6:c.819T>G
|
NP_000305.3:p.Phe273Leu
|
|
|
NM_001304717.2:c.1338T>G
|
NP_001291646.2:p.Phe446Leu
|
|
|
NM_001304718.1:c.228T>G
|
NP_001291647.1:p.Phe76Leu
|
|
|
XM_006717926.2:c.774T>G
|
XP_006717989.1:p.Phe258Leu
|
|
|
XM_011539981.1:c.819T>G
|
XP_011538283.1:p.Phe273Leu
|
|
|
XM_011539982.1:c.723T>G
|
XP_011538284.1:p.Phe241Leu
|
|
|
XR_945791.1:n.1389T>G
|
|
|
|
NM_000314.7:c.819T>G
|
NP_000305.3:p.Phe273Leu
|
|
|
NM_001304717.5:c.1338T>G
|
NP_001291646.4:p.Phe446Leu
|
|
|
NM_001304718.2:c.228T>G
|
NP_001291647.1:p.Phe76Leu
|
|
|
NM_000314.8:c.819T>G
MANE Select
|
NP_000305.3:p.Phe273Leu
|
|
