ENST00000334785.12:c.1580A>G
MANE Select
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ENSP00000333938.7:p.Glu527Gly
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ENST00000330010.12:c.1388A>G
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ENSP00000327363.8:p.Glu463Gly
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ENST00000334785.11:c.1580A>G
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ENSP00000333938.7:p.Glu527Gly
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ENST00000342754.5:c.1279A>G
|
|
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ENST00000470735.1:n.419A>G
|
|
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ENST00000480732.2:n.1154A>G
|
|
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NM_001172309.1:c.1388A>G
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NP_001165780.1:p.Glu463Gly
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NM_144573.3:c.1580A>G , LRG_442t1:c.1580A>G
|
NP_653174.3:p.Glu527Gly
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XM_005271322.2:c.1580A>G
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XP_005271379.1:p.Glu527Gly
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XM_005271323.2:c.1538A>G
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XP_005271380.1:p.Glu513Gly
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XM_005271324.3:c.1388A>G
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XP_005271381.1:p.Glu463Gly
|
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XM_005271325.2:c.1358A>G
|
XP_005271382.1:p.Glu453Gly
|
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XM_005271326.2:c.1346A>G
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XP_005271383.1:p.Glu449Gly
|
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XM_005271327.2:c.1163A>G
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XP_005271384.1:p.Glu388Gly
|
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XM_005271322.4:c.1580A>G
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XP_005271379.1:p.Glu527Gly
|
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XM_005271323.4:c.1538A>G
|
XP_005271380.1:p.Glu513Gly
|
|
XM_005271324.5:c.1388A>G
|
XP_005271381.1:p.Glu463Gly
|
|
XM_005271325.4:c.1358A>G
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XP_005271382.1:p.Glu453Gly
|
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XM_005271326.4:c.1346A>G
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XP_005271383.1:p.Glu449Gly
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|
XM_005271327.4:c.1163A>G
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XP_005271384.1:p.Glu388Gly
|
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NM_001172309.2:c.1388A>G
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NP_001165780.1:p.Glu463Gly
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NM_144573.4:c.1580A>G
MANE Select
|
NP_653174.3:p.Glu527Gly
|
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