ENST00000347147.9:c.1019C>A
MANE Select
|
ENSP00000333355.6:p.Ala340Glu
|
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ENST00000347147.8:c.1019C>A
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ENSP00000333355.6:p.Ala340Glu
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ENST00000381975.7:c.1018-3C>A
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ENSP00000371402.3:n.1018-3C>A
|
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ENST00000392432.6:c.1160C>A
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ENSP00000376227.2:p.Ala387Glu
|
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ENST00000419280.5:c.*315C>A
|
ENSP00000414077.1:n.*315C>A
|
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ENST00000429560.1:c.214-3C>A
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ENSP00000403053.1:n.214-3C>A
|
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ENST00000432352.5:c.293C>A
|
ENSP00000409963.1:p.Ala98Glu
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ENST00000452358.5:c.518C>A
|
ENSP00000414333.1:p.Ala173Glu
|
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ENST00000467284.1:n.65C>A
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|
|
ENST00000473092.5:c.1019C>A
|
ENSP00000418674.1:p.Ala340Glu
|
|
ENST00000477651.5:n.783C>A
|
|
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NM_001011655.2:c.1019C>A
|
NP_001011655.1:p.Ala340Glu
|
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NM_001166305.1:c.1160C>A
|
NP_001159777.1:p.Ala387Glu
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NM_001166306.1:c.1018-3C>A
|
NP_001159778.1:n.1018-3C>A
|
|
NM_138399.4:c.1019C>A
|
NP_612408.3:p.Ala340Glu
|
|
XM_005269371.3:c.1019C>A
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XP_005269428.1:p.Ala340Glu
|
|
XM_011513318.1:c.1169C>A
|
XP_011511620.1:p.Ala390Glu
|
|
XM_011513319.1:c.1106C>A
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XP_011511621.1:p.Ala369Glu
|
|
XM_011513320.1:c.1217C>A
|
XP_011511622.1:p.Ala406Glu
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XM_011513321.1:c.1085C>A
|
XP_011511623.1:p.Ala362Glu
|
|
XM_011513322.1:c.1076C>A
|
XP_011511624.1:p.Ala359Glu
|
|
XM_011513323.1:c.914C>A
|
XP_011511625.1:p.Ala305Glu
|
|
XM_005269371.4:c.1019C>A
|
XP_005269428.1:p.Ala340Glu
|
|
XM_011513318.2:c.1169C>A
|
XP_011511620.1:p.Ala390Glu
|
|
XM_011513319.2:c.1106C>A
|
XP_011511621.1:p.Ala369Glu
|
|
XM_011513320.2:c.1217C>A
|
XP_011511622.1:p.Ala406Glu
|
|
XM_011513321.2:c.1085C>A
|
XP_011511623.1:p.Ala362Glu
|
|
XM_011513322.2:c.1076C>A
|
XP_011511624.1:p.Ala359Glu
|
|
XM_017007517.1:c.1028C>A
|
XP_016863006.1:p.Ala343Glu
|
|
XM_017007518.1:c.1028C>A
|
XP_016863007.1:p.Ala343Glu
|
|
NM_001011655.3:c.1019C>A
MANE Select
|
NP_001011655.1:p.Ala340Glu
|
|
NM_001166305.2:c.1160C>A
|
NP_001159777.1:p.Ala387Glu
|
|
NM_001166306.2:c.1018-3C>A
|
NP_001159778.1:n.1018-3C>A
|
|
NM_138399.5:c.1019C>A
|
NP_612408.3:p.Ala340Glu
|
|