ENST00000330342.8:c.1049G>T
MANE Select
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ENSP00000332247.2:p.Gly350Val
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ENST00000540368.6:n.1080G>T
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ENST00000674794.1:c.1137G>T
|
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ENST00000675260.1:n.324G>T
|
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ENST00000675344.1:c.*70G>T
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ENSP00000501953.1:n.*70G>T
|
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ENST00000330342.7:c.1049G>T
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ENSP00000332247.2:p.Gly350Val
|
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ENST00000504192.2:c.659G>T
|
ENSP00000443441.1:p.Gly220Val
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ENST00000536426.1:n.66G>T
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ENST00000545059.5:n.3685G>T
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NM_012463.3:c.1049G>T
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NP_036595.2:p.Gly350Val
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XM_005253563.1:c.1049G>T
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XP_005253620.1:p.Gly350Val
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XM_006719317.2:c.536G>T
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XP_006719380.1:p.Gly179Val
|
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XM_006719318.2:c.227G>T
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XP_006719381.1:p.Gly76Val
|
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XR_429088.1:n.1212G>T
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|
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XM_024448910.1:c.1049G>T
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XP_024304678.1:p.Gly350Val
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XM_024448911.1:c.536G>T
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XP_024304679.1:p.Gly179Val
|
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XM_024448912.1:c.227G>T
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XP_024304680.1:p.Gly76Val
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NM_012463.4:c.1049G>T
MANE Select
|
NP_036595.2:p.Gly350Val
|
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