ENST00000347147.9:c.1067G>T
MANE Select
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ENSP00000333355.6:p.Gly356Val
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ENST00000347147.8:c.1067G>T
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ENSP00000333355.6:p.Gly356Val
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ENST00000381975.7:c.1063G>T
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ENSP00000371402.3:p.Glu355Ter
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ENST00000392432.6:c.1208G>T
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ENSP00000376227.2:p.Gly403Val
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ENST00000419280.5:c.*363G>T
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ENSP00000414077.1:n.*363G>T
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ENST00000429560.1:c.259G>T
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ENSP00000403053.1:p.Glu87Ter
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ENST00000432352.5:c.341G>T
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ENSP00000409963.1:p.Gly114Val
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ENST00000452358.5:c.566G>T
|
ENSP00000414333.1:p.Gly189Val
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ENST00000467284.1:n.113G>T
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ENST00000473092.5:c.1067G>T
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ENSP00000418674.1:p.Gly356Val
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ENST00000477651.5:n.831G>T
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NM_001011655.2:c.1067G>T
|
NP_001011655.1:p.Gly356Val
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NM_001166305.1:c.1208G>T
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NP_001159777.1:p.Gly403Val
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|
NM_001166306.1:c.1063G>T
|
NP_001159778.1:p.Glu355Ter
|
|
NM_138399.4:c.1067G>T
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NP_612408.3:p.Gly356Val
|
|
XM_005269371.3:c.1067G>T
|
XP_005269428.1:p.Gly356Val
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XM_011513318.1:c.1217G>T
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XP_011511620.1:p.Gly406Val
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XM_011513319.1:c.1154G>T
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XP_011511621.1:p.Gly385Val
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XM_011513320.1:c.1265G>T
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XP_011511622.1:p.Gly422Val
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|
XM_011513321.1:c.1133G>T
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XP_011511623.1:p.Gly378Val
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|
XM_011513322.1:c.1124G>T
|
XP_011511624.1:p.Gly375Val
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XM_011513323.1:c.962G>T
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XP_011511625.1:p.Gly321Val
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XM_005269371.4:c.1067G>T
|
XP_005269428.1:p.Gly356Val
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|
XM_011513318.2:c.1217G>T
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XP_011511620.1:p.Gly406Val
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|
XM_011513319.2:c.1154G>T
|
XP_011511621.1:p.Gly385Val
|
|
XM_011513320.2:c.1265G>T
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XP_011511622.1:p.Gly422Val
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|
XM_011513321.2:c.1133G>T
|
XP_011511623.1:p.Gly378Val
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|
XM_011513322.2:c.1124G>T
|
XP_011511624.1:p.Gly375Val
|
|
XM_017007517.1:c.1076G>T
|
XP_016863006.1:p.Gly359Val
|
|
XM_017007518.1:c.1076G>T
|
XP_016863007.1:p.Gly359Val
|
|
NM_001011655.3:c.1067G>T
MANE Select
|
NP_001011655.1:p.Gly356Val
|
|
NM_001166305.2:c.1208G>T
|
NP_001159777.1:p.Gly403Val
|
|
NM_001166306.2:c.1063G>T
|
NP_001159778.1:p.Glu355Ter
|
|
NM_138399.5:c.1067G>T
|
NP_612408.3:p.Gly356Val
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