ENST00000347147.9:c.1022G>T
MANE Select
|
ENSP00000333355.6:p.Gly341Val
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ENST00000347147.8:c.1022G>T
|
ENSP00000333355.6:p.Gly341Val
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ENST00000381975.7:c.1018G>T
|
ENSP00000371402.3:p.Ala340Ser
|
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ENST00000392432.6:c.1163G>T
|
ENSP00000376227.2:p.Gly388Val
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ENST00000419280.5:c.*318G>T
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ENSP00000414077.1:n.*318G>T
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ENST00000429560.1:c.214G>T
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ENSP00000403053.1:p.Ala72Ser
|
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ENST00000432352.5:c.296G>T
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ENSP00000409963.1:p.Gly99Val
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ENST00000452358.5:c.521G>T
|
ENSP00000414333.1:p.Gly174Val
|
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ENST00000467284.1:n.68G>T
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|
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ENST00000473092.5:c.1022G>T
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ENSP00000418674.1:p.Gly341Val
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ENST00000477651.5:n.786G>T
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|
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NM_001011655.2:c.1022G>T
|
NP_001011655.1:p.Gly341Val
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NM_001166305.1:c.1163G>T
|
NP_001159777.1:p.Gly388Val
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|
NM_001166306.1:c.1018G>T
|
NP_001159778.1:p.Ala340Ser
|
|
NM_138399.4:c.1022G>T
|
NP_612408.3:p.Gly341Val
|
|
XM_005269371.3:c.1022G>T
|
XP_005269428.1:p.Gly341Val
|
|
XM_011513318.1:c.1172G>T
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XP_011511620.1:p.Gly391Val
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XM_011513319.1:c.1109G>T
|
XP_011511621.1:p.Gly370Val
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XM_011513320.1:c.1220G>T
|
XP_011511622.1:p.Gly407Val
|
|
XM_011513321.1:c.1088G>T
|
XP_011511623.1:p.Gly363Val
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|
XM_011513322.1:c.1079G>T
|
XP_011511624.1:p.Gly360Val
|
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XM_011513323.1:c.917G>T
|
XP_011511625.1:p.Gly306Val
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XM_005269371.4:c.1022G>T
|
XP_005269428.1:p.Gly341Val
|
|
XM_011513318.2:c.1172G>T
|
XP_011511620.1:p.Gly391Val
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|
XM_011513319.2:c.1109G>T
|
XP_011511621.1:p.Gly370Val
|
|
XM_011513320.2:c.1220G>T
|
XP_011511622.1:p.Gly407Val
|
|
XM_011513321.2:c.1088G>T
|
XP_011511623.1:p.Gly363Val
|
|
XM_011513322.2:c.1079G>T
|
XP_011511624.1:p.Gly360Val
|
|
XM_017007517.1:c.1031G>T
|
XP_016863006.1:p.Gly344Val
|
|
XM_017007518.1:c.1031G>T
|
XP_016863007.1:p.Gly344Val
|
|
NM_001011655.3:c.1022G>T
MANE Select
|
NP_001011655.1:p.Gly341Val
|
|
NM_001166305.2:c.1163G>T
|
NP_001159777.1:p.Gly388Val
|
|
NM_001166306.2:c.1018G>T
|
NP_001159778.1:p.Ala340Ser
|
|
NM_138399.5:c.1022G>T
|
NP_612408.3:p.Gly341Val
|
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