ENST00000682565.1:c.10192C>G
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ENSP00000507671.1:p.His3398Asp
|
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ENST00000682801.1:c.10192C>G
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ENSP00000507862.1:p.His3398Asp
|
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ENST00000682859.1:c.10192C>G
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ENSP00000508222.1:p.His3398Asp
|
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ENST00000683791.1:c.3278C>G
|
|
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ENST00000684460.1:c.7473C>G
|
|
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ENST00000684548.1:c.10192C>G
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ENSP00000507421.1:p.His3398Asp
|
|
ENST00000684590.1:c.4639C>G
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ENSP00000507376.1:p.His1547Asp
|
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ENST00000684656.1:c.7518C>G
|
|
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ENST00000613296.6:c.10573C>G
MANE Select
|
ENSP00000482968.1:p.His3525Asp
|
|
ENST00000651057.1:c.727C>G
|
ENSP00000498504.1:p.His243Asp
|
|
ENST00000651434.1:c.1929C>G
|
|
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ENST00000652487.1:c.1670C>G
|
|
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ENST00000423048.5:c.4064C>G
|
ENSP00000399833.1:n.4064C>G
|
|
ENST00000484298.5:c.10447C>G
|
ENSP00000478155.1:p.His3483Asp
|
|
ENST00000613296.4:c.10573C>G
|
ENSP00000482968.1:p.His3525Asp
|
|
ENST00000614410.4:c.10573C>G
|
ENSP00000479094.1:p.His3525Asp
|
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ENST00000620466.4:n.4376C>G
|
|
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NM_015120.4:c.10576C>G , LRG_741t1:c.10576C>G
|
NP_055935.4:p.His3526Asp
|
|
NM_001378454.1:c.10573C>G
MANE Select
|
NP_001365383.1:p.His3525Asp
|
|