|
ENST00000700029.2:c.773T>A
|
ENSP00000514759.2:p.Phe258Tyr
|
|
|
ENST00000710265.1:c.773T>A
|
ENSP00000518161.1:p.Phe258Tyr
|
|
|
ENST00000472832.3:c.773T>A
|
ENSP00000483066.2:p.Phe258Tyr
|
|
|
ENST00000688158.2:n.1508T>A
|
|
|
|
ENST00000688922.2:c.*603T>A
|
ENSP00000508742.2:n.*603T>A
|
|
|
ENST00000700021.1:c.728T>A
|
ENSP00000514757.1:p.Phe243Tyr
|
|
|
ENST00000700022.1:c.*112T>A
|
ENSP00000514758.1:n.*112T>A
|
|
|
ENST00000700023.1:n.1931T>A
|
|
|
|
ENST00000700024.1:n.2165T>A
|
|
|
|
ENST00000700025.1:n.1542T>A
|
|
|
|
ENST00000700026.1:n.410T>A
|
|
|
|
ENST00000700029.1:c.607T>A
|
|
|
|
ENST00000706954.1:c.773T>A
|
ENSP00000516674.1:p.Phe258Tyr
|
|
|
ENST00000706955.1:c.*808T>A
|
ENSP00000516675.1:n.*808T>A
|
|
|
ENST00000686459.1:c.*359T>A
|
ENSP00000508909.1:n.*359T>A
|
|
|
ENST00000688158.1:c.*884T>A
|
ENSP00000509254.1:n.*884T>A
|
|
|
ENST00000688308.1:c.773T>A
|
ENSP00000508752.1:p.Phe258Tyr
|
|
|
ENST00000688922.1:c.694T>A
|
|
|
|
ENST00000693560.1:c.1292T>A
|
ENSP00000509861.1:p.Phe431Tyr
|
|
|
ENST00000371953.8:c.773T>A
MANE Select
|
ENSP00000361021.3:p.Phe258Tyr
|
|
|
ENST00000371953.7:c.773T>A
|
ENSP00000361021.3:p.Phe258Tyr
|
|
|
ENST00000472832.2:c.200T>A
|
ENSP00000483066.1:p.Phe67Tyr
|
|
|
NM_000314.5:c.773T>A
|
NP_000305.3:p.Phe258Tyr
|
|
|
NM_000314.6:c.773T>A
|
NP_000305.3:p.Phe258Tyr
|
|
|
NM_001304717.2:c.1292T>A
|
NP_001291646.2:p.Phe431Tyr
|
|
|
NM_001304718.1:c.182T>A
|
NP_001291647.1:p.Phe61Tyr
|
|
|
XM_006717926.2:c.728T>A
|
XP_006717989.1:p.Phe243Tyr
|
|
|
XM_011539981.1:c.773T>A
|
XP_011538283.1:p.Phe258Tyr
|
|
|
XM_011539982.1:c.677T>A
|
XP_011538284.1:p.Phe226Tyr
|
|
|
XR_945791.1:n.1343T>A
|
|
|
|
NM_000314.7:c.773T>A
|
NP_000305.3:p.Phe258Tyr
|
|
|
NM_001304717.5:c.1292T>A
|
NP_001291646.4:p.Phe431Tyr
|
|
|
NM_001304718.2:c.182T>A
|
NP_001291647.1:p.Phe61Tyr
|
|
|
NM_000314.8:c.773T>A
MANE Select
|
NP_000305.3:p.Phe258Tyr
|
|
