ENST00000219548.9:c.513G>T
(STUB1)
MANE Select
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ENSP00000219548.4:p.Ala171=
|
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ENST00000219548.8:c.513G>T
(STUB1)
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ENSP00000219548.4:p.Ala171=
|
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ENST00000563505.5:n.609G>T
(STUB1)
|
|
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ENST00000564316.1:c.112G>T
(STUB1)
|
|
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ENST00000564370.5:c.297G>T
(STUB1)
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ENSP00000456875.1:p.Ala99=
|
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ENST00000565677.5:c.297G>T
(STUB1)
|
ENSP00000457228.1:p.Ala99=
|
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ENST00000566181.2:n.282G>T
(STUB1)
|
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ENST00000566408.5:c.230G>T
(STUB1)
|
|
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ENST00000567173.5:c.456G>T
(STUB1)
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ENSP00000456591.1:p.Ala152=
|
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ENST00000569248.5:n.1087G>T
(STUB1)
|
|
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ENST00000620831.4:c.-50+38289G>T
(MSLN)
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ENSP00000482893.1:n.-50+38289G>T
|
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NM_001293197.1:c.297G>T
(STUB1)
|
NP_001280126.1:p.Ala99=
|
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NM_005861.3:c.513G>T
(STUB1)
|
NP_005852.2:p.Ala171=
|
|
NM_005861.4:c.513G>T
(STUB1)
MANE Select
|
NP_005852.2:p.Ala171=
|
|
NM_001293197.2:c.297G>T
(STUB1)
|
NP_001280126.1:p.Ala99=
|
|