ENST00000542672.7:c.1494G>T
|
ENSP00000443495.1:p.Gln498His
|
|
ENST00000492634.7:n.1424G>T
|
|
|
ENST00000682015.1:c.1401G>T
|
ENSP00000506961.1:p.Gln467His
|
|
ENST00000682692.1:n.1241G>T
|
|
|
ENST00000682966.1:n.7135G>T
|
|
|
ENST00000683111.1:c.*780G>T
|
ENSP00000507913.1:n.*780G>T
|
|
ENST00000683322.1:n.2846G>T
|
|
|
ENST00000684050.1:n.4132G>T
|
|
|
ENST00000684286.1:n.3049G>T
|
|
|
ENST00000684502.1:n.1443G>T
|
|
|
ENST00000366578.6:c.1494G>T
MANE Select
|
ENSP00000355537.4:p.Gln498His
|
|
ENST00000492634.6:n.1424G>T
|
|
|
ENST00000542672.6:c.1494G>T
|
ENSP00000443495.1:p.Gln498His
|
|
ENST00000651091.1:c.1184G>T
|
ENSP00000498677.1:n.1184G>T
|
|
ENST00000651275.1:c.1386G>T
|
ENSP00000498926.1:p.Gln462His
|
|
ENST00000651781.1:c.574G>T
|
|
|
ENST00000651786.1:c.*866G>T
|
ENSP00000498364.1:n.*866G>T
|
|
ENST00000652096.1:c.*899G>T
|
ENSP00000498896.1:n.*899G>T
|
|
ENST00000366578.5:c.1494G>T
|
ENSP00000355537.4:p.Gln498His
|
|
ENST00000492101.1:n.55G>T
|
|
|
ENST00000542672.5:c.1494G>T
|
ENSP00000443495.1:p.Gln498His
|
|
ENST00000546208.5:c.870G>T
|
ENSP00000438384.2:p.Gln290His
|
|
NM_001103.3:c.1494G>T
|
NP_001094.1:p.Gln498His
|
|
NM_001278343.1:c.1494G>T
|
NP_001265272.1:p.Gln498His
|
|
NM_001278344.1:c.870G>T
|
NP_001265273.1:p.Gln290His
|
|
NM_001278343.2:c.1494G>T
|
NP_001265272.1:p.Gln498His
|
|
NM_001103.4:c.1494G>T
MANE Select
|
NP_001094.1:p.Gln498His
|
|
NM_001278344.2:c.870G>T
|
NP_001265273.1:p.Gln290His
|
|