|
ENST00000700029.2:c.925T>A
|
ENSP00000514759.2:p.Phe309Ile
|
|
|
ENST00000710265.1:c.832T>A
|
ENSP00000518161.1:p.Phe278Ile
|
|
|
ENST00000472832.3:c.832T>A
|
ENSP00000483066.2:p.Phe278Ile
|
|
|
ENST00000688158.2:n.1567T>A
|
|
|
|
ENST00000688922.2:c.*662T>A
|
ENSP00000508742.2:n.*662T>A
|
|
|
ENST00000700021.1:c.787T>A
|
ENSP00000514757.1:p.Phe263Ile
|
|
|
ENST00000700022.1:c.*171T>A
|
ENSP00000514758.1:n.*171T>A
|
|
|
ENST00000700023.1:n.1990T>A
|
|
|
|
ENST00000700024.1:n.2224T>A
|
|
|
|
ENST00000700025.1:n.1601T>A
|
|
|
|
ENST00000700026.1:n.469T>A
|
|
|
|
ENST00000700029.1:c.759T>A
|
|
|
|
ENST00000706954.1:c.832T>A
|
ENSP00000516674.1:p.Phe278Ile
|
|
|
ENST00000706955.1:c.*867T>A
|
ENSP00000516675.1:n.*867T>A
|
|
|
ENST00000686459.1:c.*418T>A
|
ENSP00000508909.1:n.*418T>A
|
|
|
ENST00000688158.1:c.*943T>A
|
ENSP00000509254.1:n.*943T>A
|
|
|
ENST00000688308.1:c.832T>A
|
ENSP00000508752.1:p.Phe278Ile
|
|
|
ENST00000688922.1:c.753T>A
|
|
|
|
ENST00000693560.1:c.1351T>A
|
ENSP00000509861.1:p.Phe451Ile
|
|
|
ENST00000371953.8:c.832T>A
MANE Select
|
ENSP00000361021.3:p.Phe278Ile
|
|
|
ENST00000371953.7:c.832T>A
|
ENSP00000361021.3:p.Phe278Ile
|
|
|
ENST00000472832.2:c.259T>A
|
ENSP00000483066.1:p.Phe87Ile
|
|
|
NM_000314.5:c.832T>A
|
NP_000305.3:p.Phe278Ile
|
|
|
NM_000314.6:c.832T>A
|
NP_000305.3:p.Phe278Ile
|
|
|
NM_001304717.2:c.1351T>A
|
NP_001291646.2:p.Phe451Ile
|
|
|
NM_001304718.1:c.241T>A
|
NP_001291647.1:p.Phe81Ile
|
|
|
XM_006717926.2:c.787T>A
|
XP_006717989.1:p.Phe263Ile
|
|
|
XM_011539981.1:c.832T>A
|
XP_011538283.1:p.Phe278Ile
|
|
|
XM_011539982.1:c.736T>A
|
XP_011538284.1:p.Phe246Ile
|
|
|
XR_945791.1:n.1402T>A
|
|
|
|
NM_000314.7:c.832T>A
|
NP_000305.3:p.Phe278Ile
|
|
|
NM_001304717.5:c.1351T>A
|
NP_001291646.4:p.Phe451Ile
|
|
|
NM_001304718.2:c.241T>A
|
NP_001291647.1:p.Phe81Ile
|
|
|
NM_000314.8:c.832T>A
MANE Select
|
NP_000305.3:p.Phe278Ile
|
|
