ENST00000369626.8:c.744_750delinsAATTAAT
MANE Select
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ENSP00000358640.4:p.Thr248=
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ENST00000429288.2:c.744_750delinsAATTAAT
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ENSP00000397106.2:p.Thr248=
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ENST00000443580.6:c.744_750delinsAATTAAT
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ENSP00000399104.2:p.Thr248=
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ENST00000458229.6:c.744_750delinsAATTAAT
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ENSP00000416167.2:p.Thr248=
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ENST00000679803.1:c.744_750delinsAATTAAT
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ENSP00000505879.1:p.Thr248=
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ENST00000679846.1:n.1661_1667delinsAATTAAT
|
|
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ENST00000369626.7:c.744_750delinsAATTAAT
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ENSP00000358640.3:p.Thr248=
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ENST00000443580.5:c.744_750delinsAATTAAT
|
ENSP00000399104.1:p.Thr248=
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|
ENST00000458229.5:c.744_750delinsAATTAAT
|
ENSP00000416167.1:p.Thr248=
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|
ENST00000538576.5:c.744_750delinsAATTAAT
|
ENSP00000441065.1:p.Thr248=
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|
NM_001166496.1:c.744_750delinsAATTAAT
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NP_001159968.1:p.Thr248=
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|
NM_003051.3:c.744_750delinsAATTAAT
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NP_003042.3:p.Thr248=
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|
XM_011542026.1:c.744_750delinsAATTAAT
|
XP_011540328.1:p.Thr248=
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|
XM_011542027.1:c.744_750delinsAATTAAT
|
XP_011540329.1:p.Thr248=
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|
NM_003051.4:c.744_750delinsAATTAAT
MANE Select
|
NP_003042.3:p.Thr248=
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|
NM_001166496.2:c.744_750delinsAATTAAT
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NP_001159968.1:p.Thr248=
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