ENST00000334785.12:c.1407A>G
MANE Select
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ENSP00000333938.7:p.Glu469=
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ENST00000330010.12:c.1215A>G
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ENSP00000327363.8:p.Glu405=
|
|
ENST00000334785.11:c.1407A>G
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ENSP00000333938.7:p.Glu469=
|
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ENST00000342754.5:c.1106A>G
|
|
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ENST00000480732.2:n.981A>G
|
|
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NM_001172309.1:c.1215A>G
|
NP_001165780.1:p.Glu405=
|
|
NM_144573.3:c.1407A>G , LRG_442t1:c.1407A>G
|
NP_653174.3:p.Glu469=
|
|
XM_005271322.2:c.1407A>G
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XP_005271379.1:p.Glu469=
|
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XM_005271323.2:c.1365A>G
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XP_005271380.1:p.Glu455=
|
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XM_005271324.3:c.1215A>G
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XP_005271381.1:p.Glu405=
|
|
XM_005271325.2:c.1251+2499A>G
|
XP_005271382.1:n.1251+2499A>G
|
|
XM_005271326.2:c.1173A>G
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XP_005271383.1:p.Glu391=
|
|
XM_005271327.2:c.990A>G
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XP_005271384.1:p.Glu330=
|
|
XM_005271322.4:c.1407A>G
|
XP_005271379.1:p.Glu469=
|
|
XM_005271323.4:c.1365A>G
|
XP_005271380.1:p.Glu455=
|
|
XM_005271324.5:c.1215A>G
|
XP_005271381.1:p.Glu405=
|
|
XM_005271325.4:c.1251+2499A>G
|
XP_005271382.1:n.1251+2499A>G
|
|
XM_005271326.4:c.1173A>G
|
XP_005271383.1:p.Glu391=
|
|
XM_005271327.4:c.990A>G
|
XP_005271384.1:p.Glu330=
|
|
NM_001172309.2:c.1215A>G
|
NP_001165780.1:p.Glu405=
|
|
NM_144573.4:c.1407A>G
MANE Select
|
NP_653174.3:p.Glu469=
|
|