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NM_001378454.1:c.784G>T
MANE Select
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NP_001365383.1:p.Glu262Ter
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|
ENST00000613296.6:c.784G>T
MANE Select
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ENSP00000482968.1:p.Glu262Ter
|
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NM_015120.4:c.787G>T , LRG_741t1:c.787G>T
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NP_055935.4:p.Glu263Ter
|
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ENST00000484298.5:c.658G>T
|
ENSP00000478155.1:p.Glu220Ter
|
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ENST00000613296.4:c.784G>T
|
ENSP00000482968.1:p.Glu262Ter
|
|
ENST00000614410.4:c.784G>T
|
ENSP00000479094.1:p.Glu262Ter
|
|
ENST00000682565.1:c.334G>T
|
ENSP00000507671.1:p.Glu112Ter
|
|
ENST00000682675.1:n.744G>T
|
|
|
ENST00000682801.1:c.334G>T
|
ENSP00000507862.1:p.Glu112Ter
|
|
ENST00000682859.1:c.334G>T
|
ENSP00000508222.1:p.Glu112Ter
|
|
ENST00000682889.1:n.749G>T
|
|
|
ENST00000683791.1:c.138G>T
|
|
|
ENST00000684548.1:c.334G>T
|
ENSP00000507421.1:p.Glu112Ter
|