ENST00000330342.8:c.1181T>G
MANE Select
|
ENSP00000332247.2:p.Val394Gly
|
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ENST00000540368.6:n.1212T>G
|
|
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ENST00000674794.1:c.1269T>G
|
|
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ENST00000675260.1:n.456T>G
|
|
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ENST00000675344.1:c.*202T>G
|
ENSP00000501953.1:n.*202T>G
|
|
ENST00000330342.7:c.1181T>G
|
ENSP00000332247.2:p.Val394Gly
|
|
ENST00000504192.2:c.791T>G
|
ENSP00000443441.1:p.Val264Gly
|
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ENST00000536426.1:n.198T>G
|
|
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ENST00000545059.5:n.3817T>G
|
|
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NM_012463.3:c.1181T>G
|
NP_036595.2:p.Val394Gly
|
|
XM_005253563.1:c.1181T>G
|
XP_005253620.1:p.Val394Gly
|
|
XM_006719317.2:c.668T>G
|
XP_006719380.1:p.Val223Gly
|
|
XM_006719318.2:c.359T>G
|
XP_006719381.1:p.Val120Gly
|
|
XR_429088.1:n.1344T>G
|
|
|
XM_024448910.1:c.1181T>G
|
XP_024304678.1:p.Val394Gly
|
|
XM_024448911.1:c.668T>G
|
XP_024304679.1:p.Val223Gly
|
|
XM_024448912.1:c.359T>G
|
XP_024304680.1:p.Val120Gly
|
|
NM_012463.4:c.1181T>G
MANE Select
|
NP_036595.2:p.Val394Gly
|
|