ENST00000704350.1:c.3285A>T
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ENSP00000515861.1:p.Ala1095=
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ENST00000704352.1:c.1174-45676A>T
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ENSP00000515863.1:n.1174-45676A>T
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ENST00000704353.1:c.1174-45676A>T
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ENSP00000515864.1:n.1174-45676A>T
|
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ENST00000704354.1:c.3629A>T
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|
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ENST00000704355.1:c.2009A>T
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|
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ENST00000349721.8:c.3645A>T
MANE Select
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ENSP00000265773.5:p.Ala1215=
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ENST00000357248.8:c.3645A>T
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ENSP00000349788.2:p.Ala1215=
|
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ENST00000635739.1:n.2313A>T
|
|
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ENST00000636157.1:n.1252A>T
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|
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ENST00000638139.1:n.679A>T
|
|
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ENST00000349721.7:c.3645A>T
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ENSP00000265773.5:p.Ala1215=
|
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ENST00000357248.7:c.3645A>T
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ENSP00000349788.2:p.Ala1215=
|
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ENST00000382194.6:c.3645A>T
|
ENSP00000371629.1:p.Ala1215=
|
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ENST00000382203.5:c.3645A>T
|
ENSP00000371638.1:p.Ala1215=
|
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ENST00000450198.6:c.3471A>T
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ENSP00000392081.2:p.Ala1157=
|
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ENST00000634760.1:c.3645A>T
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ENSP00000489256.1:p.Ala1215=
|
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ENST00000634772.1:c.62-3448A>T
|
|
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ENST00000634925.1:n.1136A>T
|
|
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NM_001289396.1:c.3645A>T
|
NP_001276325.1:p.Ala1215=
|
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NM_001289397.1:c.3471A>T
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NP_001276326.1:p.Ala1157=
|
|
NM_003070.4:c.3645A>T
|
NP_003061.3:p.Ala1215=
|
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NM_139045.3:c.3645A>T
|
NP_620614.2:p.Ala1215=
|
|
NM_003070.5:c.3645A>T
MANE Select
|
NP_003061.3:p.Ala1215=
|
|
NM_001289397.2:c.3471A>T
|
NP_001276326.1:p.Ala1157=
|
|
NM_139045.4:c.3645A>T
|
NP_620614.2:p.Ala1215=
|
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