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NM_000138.5:c.7822G>T
MANE Select
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NP_000129.3:p.Glu2608Ter
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ENST00000316623.10:c.7822G>T
MANE Select
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ENSP00000325527.5:p.Glu2608Ter
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NM_000138.4:c.7822G>T , LRG_778t1:c.7822G>T
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NP_000129.3:p.Glu2608Ter
|
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ENST00000316623.9:c.7822G>T
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ENSP00000325527.5:p.Glu2608Ter
|
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ENST00000559133.5:c.3191G>T
|
|
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ENST00000559133.6:c.*630G>T
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ENSP00000453958.2:n.*630G>T
|
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ENST00000561429.1:n.77G>T
|
|
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ENST00000674301.1:c.2988G>T
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ENSP00000501333.1:n.2988G>T
|
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ENST00000674301.2:c.*1335G>T
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ENSP00000501333.2:n.*1335G>T
|
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ENST00000682158.1:n.1203G>T
|
|
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ENST00000682170.1:n.2003G>T
|
|
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ENST00000682767.1:n.1119G>T
|
|