ENST00000355832.10:c.1692G>A
MANE Select
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ENSP00000348089.5:p.Glu564=
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ENST00000681632.1:n.1770G>A
|
|
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ENST00000681659.1:c.1533G>A
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ENSP00000505631.1:p.Glu511=
|
|
ENST00000355832.9:c.1692G>A
|
ENSP00000348089.5:p.Glu564=
|
|
ENST00000475116.1:n.275+7292G>A
|
|
|
ENST00000623073.3:c.93G>A
|
ENSP00000485650.1:p.Glu31=
|
|
ENST00000623115.3:c.-70+7292G>A
|
ENSP00000485321.1:n.-70+7292G>A
|
|
ENST00000623318.1:c.93G>A
|
ENSP00000485423.1:p.Glu31=
|
|
NM_000124.3:c.1692G>A
|
NP_000115.1:p.Glu564=
|
|
NM_001346440.1:c.1692G>A
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NP_001333369.1:p.Glu564=
|
|
NM_000124.4:c.1692G>A
MANE Select
|
NP_000115.1:p.Glu564=
|
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NM_001346440.2:c.1692G>A
|
NP_001333369.1:p.Glu564=
|
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