ENST00000334785.12:c.1460A=
MANE Select
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ENSP00000333938.7:p.Glu487=
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ENST00000330010.12:c.1268A=
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ENSP00000327363.8:p.Glu423=
|
|
ENST00000334785.11:c.1460A=
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ENSP00000333938.7:p.Glu487=
|
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ENST00000342754.5:c.1159A=
|
|
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ENST00000480732.2:n.1034A=
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|
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NM_001172309.1:c.1268A=
|
NP_001165780.1:p.Glu423=
|
|
NM_144573.3:c.1460A= , LRG_442t1:c.1460A=
|
NP_653174.3:p.Glu487=
|
|
XM_005271322.2:c.1460A=
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XP_005271379.1:p.Glu487=
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|
XM_005271323.2:c.1418A=
|
XP_005271380.1:p.Glu473=
|
|
XM_005271324.3:c.1268A=
|
XP_005271381.1:p.Glu423=
|
|
XM_005271325.2:c.1251+2552A=
|
XP_005271382.1:n.1251+2552A=
|
|
XM_005271326.2:c.1226A=
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XP_005271383.1:p.Glu409=
|
|
XM_005271327.2:c.1043A=
|
XP_005271384.1:p.Glu348=
|
|
XM_005271322.4:c.1460A=
|
XP_005271379.1:p.Glu487=
|
|
XM_005271323.4:c.1418A=
|
XP_005271380.1:p.Glu473=
|
|
XM_005271324.5:c.1268A=
|
XP_005271381.1:p.Glu423=
|
|
XM_005271325.4:c.1251+2552A=
|
XP_005271382.1:n.1251+2552A=
|
|
XM_005271326.4:c.1226A=
|
XP_005271383.1:p.Glu409=
|
|
XM_005271327.4:c.1043A=
|
XP_005271384.1:p.Glu348=
|
|
NM_001172309.2:c.1268A=
|
NP_001165780.1:p.Glu423=
|
|
NM_144573.4:c.1460A=
MANE Select
|
NP_653174.3:p.Glu487=
|
|