ENST00000232607.7:c.368A>G
MANE Select
|
ENSP00000232607.2:p.Glu123Gly
|
|
ENST00000232607.6:c.368A>G
|
ENSP00000232607.2:p.Glu123Gly
|
|
ENST00000460034.5:c.*112A>G
|
ENSP00000420409.1:n.*112A>G
|
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ENST00000462091.5:c.*40A>G
|
ENSP00000417893.1:n.*40A>G
|
|
ENST00000467167.5:c.*266A>G
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ENSP00000419618.1:n.*266A>G
|
|
ENST00000474588.5:c.311-290A>G
|
ENSP00000420348.1:n.311-290A>G
|
|
ENST00000479719.5:c.368A>G
|
ENSP00000420754.1:p.Glu123Gly
|
|
ENST00000497791.5:c.*40A>G
|
ENSP00000419121.1:n.*40A>G
|
|
ENST00000498715.1:n.86A>G
|
|
|
NM_000373.3:c.368A>G
|
NP_000364.1:p.Glu123Gly
|
|
NR_033434.1:n.320A>G
|
|
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NR_033437.1:n.573A>G
|
|
|
XR_001740253.2:n.398A>G
|
|
|
NM_000373.4:c.368A>G
MANE Select
|
NP_000364.1:p.Glu123Gly
|
|
NR_033434.2:n.234A>G
|
|
|
NR_033437.2:n.487A>G
|
|
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