ENST00000330342.8:c.1247G>T
MANE Select
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ENSP00000332247.2:p.Gly416Val
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ENST00000540368.6:n.1278G>T
|
|
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ENST00000674794.1:c.1335G>T
|
|
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ENST00000675260.1:n.522G>T
|
|
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ENST00000675344.1:c.*268G>T
|
ENSP00000501953.1:n.*268G>T
|
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ENST00000330342.7:c.1247G>T
|
ENSP00000332247.2:p.Gly416Val
|
|
ENST00000504192.2:c.857G>T
|
ENSP00000443441.1:p.Gly286Val
|
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ENST00000536426.1:n.264G>T
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ENST00000545059.5:n.3883G>T
|
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NM_012463.3:c.1247G>T
|
NP_036595.2:p.Gly416Val
|
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XM_005253563.1:c.1247G>T
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XP_005253620.1:p.Gly416Val
|
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XM_006719317.2:c.734G>T
|
XP_006719380.1:p.Gly245Val
|
|
XM_006719318.2:c.425G>T
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XP_006719381.1:p.Gly142Val
|
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XR_429088.1:n.1410G>T
|
|
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XM_024448910.1:c.1247G>T
|
XP_024304678.1:p.Gly416Val
|
|
XM_024448911.1:c.734G>T
|
XP_024304679.1:p.Gly245Val
|
|
XM_024448912.1:c.425G>T
|
XP_024304680.1:p.Gly142Val
|
|
NM_012463.4:c.1247G>T
MANE Select
|
NP_036595.2:p.Gly416Val
|
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