ENST00000330342.8:c.1251T>A
MANE Select
|
ENSP00000332247.2:p.His417Gln
|
|
ENST00000540368.6:n.1282T>A
|
|
|
ENST00000674794.1:c.1339T>A
|
|
|
ENST00000675260.1:n.526T>A
|
|
|
ENST00000675344.1:c.*272T>A
|
ENSP00000501953.1:n.*272T>A
|
|
ENST00000330342.7:c.1251T>A
|
ENSP00000332247.2:p.His417Gln
|
|
ENST00000504192.2:c.861T>A
|
ENSP00000443441.1:p.His287Gln
|
|
ENST00000536426.1:n.268T>A
|
|
|
ENST00000545059.5:n.3887T>A
|
|
|
NM_012463.3:c.1251T>A
|
NP_036595.2:p.His417Gln
|
|
XM_005253563.1:c.1251T>A
|
XP_005253620.1:p.His417Gln
|
|
XM_006719317.2:c.738T>A
|
XP_006719380.1:p.His246Gln
|
|
XM_006719318.2:c.429T>A
|
XP_006719381.1:p.His143Gln
|
|
XR_429088.1:n.1414T>A
|
|
|
XM_024448910.1:c.1251T>A
|
XP_024304678.1:p.His417Gln
|
|
XM_024448911.1:c.738T>A
|
XP_024304679.1:p.His246Gln
|
|
XM_024448912.1:c.429T>A
|
XP_024304680.1:p.His143Gln
|
|
NM_012463.4:c.1251T>A
MANE Select
|
NP_036595.2:p.His417Gln
|
|