ENST00000472480.2:n.1085A=
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|
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ENST00000685279.1:c.-29A=
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ENSP00000509424.1:n.-29A=
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ENST00000688043.1:n.1426A=
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ENST00000689668.1:n.1212A=
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|
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ENST00000690679.1:c.1392A=
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|
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ENST00000690876.1:c.1094A=
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ENSP00000508955.1:p.Glu365=
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ENST00000691229.1:c.1094A=
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ENSP00000510437.1:p.Glu365=
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|
ENST00000692089.1:c.1094A=
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ENSP00000508626.1:p.Glu365=
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ENST00000692620.1:c.-29A=
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ENSP00000509311.1:n.-29A=
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|
ENST00000402219.8:c.1205A=
MANE Select
|
ENSP00000384675.2:p.Glu402=
|
|
ENST00000395038.6:c.1205A=
|
ENSP00000378479.2:p.Glu402=
|
|
ENST00000402219.6:c.1205A=
|
ENSP00000384675.2:p.Glu402=
|
|
ENST00000426016.5:c.1205A=
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ENSP00000387784.1:p.Glu402=
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|
ENST00000472480.1:n.49A=
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|
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NM_005633.3:c.1205A= , LRG_754t1:c.1205A=
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NP_005624.2:p.Glu402=
|
|
XM_005264515.3:c.1205A=
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XP_005264572.1:p.Glu402=
|
|
XM_011533060.1:c.1298A=
|
XP_011531362.1:p.Glu433=
|
|
XM_011533061.1:c.1298A=
|
XP_011531363.1:p.Glu433=
|
|
XM_011533062.1:c.1184A=
|
XP_011531364.1:p.Glu395=
|
|
XM_011533063.1:c.1181A=
|
XP_011531365.1:p.Glu394=
|
|
XM_011533064.1:c.1034A=
|
XP_011531366.1:p.Glu345=
|
|
XM_011533065.1:c.1298A=
|
XP_011531367.1:p.Glu433=
|
|
XM_011533066.1:c.140A=
|
XP_011531368.1:p.Glu47=
|
|
XM_005264515.4:c.1205A=
|
XP_005264572.1:p.Glu402=
|
|
XM_011533062.2:c.1184A=
|
XP_011531364.1:p.Glu395=
|
|
XM_011533064.2:c.1034A=
|
XP_011531366.1:p.Glu345=
|
|
NM_001382394.1:c.1184A=
|
NP_001369323.1:p.Glu395=
|
|
NM_001382395.1:c.1205A=
|
NP_001369324.1:p.Glu402=
|
|
NM_005633.4:c.1205A=
MANE Select
|
NP_005624.2:p.Glu402=
|
|