ENST00000330342.8:c.1393G>A
MANE Select
|
ENSP00000332247.2:p.Gly465Ser
|
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ENST00000540368.6:n.1424G>A
|
|
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ENST00000674794.1:c.1481G>A
|
|
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ENST00000675260.1:n.668G>A
|
|
|
ENST00000675344.1:c.*414G>A
|
ENSP00000501953.1:n.*414G>A
|
|
ENST00000330342.7:c.1393G>A
|
ENSP00000332247.2:p.Gly465Ser
|
|
ENST00000536426.1:n.410G>A
|
|
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ENST00000545059.5:n.4029G>A
|
|
|
NM_012463.3:c.1393G>A
|
NP_036595.2:p.Gly465Ser
|
|
XM_005253563.1:c.1393G>A
|
XP_005253620.1:p.Gly465Ser
|
|
XM_006719317.2:c.880G>A
|
XP_006719380.1:p.Gly294Ser
|
|
XM_006719318.2:c.571G>A
|
XP_006719381.1:p.Gly191Ser
|
|
XR_429088.1:n.1556G>A
|
|
|
XM_024448910.1:c.1393G>A
|
XP_024304678.1:p.Gly465Ser
|
|
XM_024448911.1:c.880G>A
|
XP_024304679.1:p.Gly294Ser
|
|
XM_024448912.1:c.571G>A
|
XP_024304680.1:p.Gly191Ser
|
|
NM_012463.4:c.1393G>A
MANE Select
|
NP_036595.2:p.Gly465Ser
|
|