ENST00000330342.8:c.1392T>G
MANE Select
|
ENSP00000332247.2:p.Thr464=
|
|
ENST00000540368.6:n.1423T>G
|
|
|
ENST00000674794.1:c.1480T>G
|
|
|
ENST00000675260.1:n.667T>G
|
|
|
ENST00000675344.1:c.*413T>G
|
ENSP00000501953.1:n.*413T>G
|
|
ENST00000330342.7:c.1392T>G
|
ENSP00000332247.2:p.Thr464=
|
|
ENST00000536426.1:n.409T>G
|
|
|
ENST00000545059.5:n.4028T>G
|
|
|
NM_012463.3:c.1392T>G
|
NP_036595.2:p.Thr464=
|
|
XM_005253563.1:c.1392T>G
|
XP_005253620.1:p.Thr464=
|
|
XM_006719317.2:c.879T>G
|
XP_006719380.1:p.Thr293=
|
|
XM_006719318.2:c.570T>G
|
XP_006719381.1:p.Thr190=
|
|
XR_429088.1:n.1555T>G
|
|
|
XM_024448910.1:c.1392T>G
|
XP_024304678.1:p.Thr464=
|
|
XM_024448911.1:c.879T>G
|
XP_024304679.1:p.Thr293=
|
|
XM_024448912.1:c.570T>G
|
XP_024304680.1:p.Thr190=
|
|
NM_012463.4:c.1392T>G
MANE Select
|
NP_036595.2:p.Thr464=
|
|