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ENST00000375254.8:c.15282T>C
MANE Select
|
ENSP00000364403.3:p.Leu5094=
|
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|
ENST00000375224.1:c.2403T>C
|
ENSP00000364372.1:p.Leu801=
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ENST00000375225.7:c.507T>C
|
ENSP00000364373.3:p.Leu169=
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ENST00000375254.7:c.15282T>C
|
ENSP00000364403.3:p.Leu5094=
|
|
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ENST00000459947.5:n.3289T>C
|
|
|
|
NM_020765.2:c.15282T>C
|
NP_065816.2:p.Leu5094=
|
|
|
XM_011541108.1:c.15435T>C
|
XP_011539410.1:p.Leu5145=
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XM_011541109.1:c.15432T>C
|
XP_011539411.1:p.Leu5144=
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XM_011541110.1:c.15432T>C
|
XP_011539412.1:p.Leu5144=
|
|
|
XM_011541111.1:c.15432T>C
|
XP_011539413.1:p.Leu5144=
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XM_011541112.1:c.15420T>C
|
XP_011539414.1:p.Leu5140=
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XM_011541113.1:c.15417T>C
|
XP_011539415.1:p.Leu5139=
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XM_011541114.1:c.15417T>C
|
XP_011539416.1:p.Leu5139=
|
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XM_011541115.1:c.15411T>C
|
XP_011539417.1:p.Leu5137=
|
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XM_011541116.1:c.15402T>C
|
XP_011539418.1:p.Leu5134=
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XM_011541117.1:c.15351T>C
|
XP_011539419.1:p.Leu5117=
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XM_011541118.1:c.15348T>C
|
XP_011539420.1:p.Leu5116=
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XM_011541119.1:c.15315T>C
|
XP_011539421.1:p.Leu5105=
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XM_011541120.1:c.15312T>C
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XP_011539422.1:p.Leu5104=
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XM_011541121.1:c.15279T>C
|
XP_011539423.1:p.Leu5093=
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XM_011541108.3:c.15549T>C
|
XP_011539410.2:p.Leu5183=
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XM_011541109.3:c.15546T>C
|
XP_011539411.2:p.Leu5182=
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XM_011541110.3:c.15546T>C
|
XP_011539412.2:p.Leu5182=
|
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XM_011541111.3:c.15546T>C
|
XP_011539413.2:p.Leu5182=
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XM_011541112.3:c.15534T>C
|
XP_011539414.2:p.Leu5178=
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XM_011541113.3:c.15531T>C
|
XP_011539415.2:p.Leu5177=
|
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XM_011541114.3:c.15531T>C
|
XP_011539416.2:p.Leu5177=
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XM_011541115.3:c.15525T>C
|
XP_011539417.2:p.Leu5175=
|
|
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XM_011541116.3:c.15516T>C
|
XP_011539418.2:p.Leu5172=
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XM_011541117.3:c.15465T>C
|
XP_011539419.2:p.Leu5155=
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XM_011541118.3:c.15462T>C
|
XP_011539420.2:p.Leu5154=
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XM_011541119.3:c.15429T>C
|
XP_011539421.2:p.Leu5143=
|
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XM_011541120.3:c.15426T>C
|
XP_011539422.2:p.Leu5142=
|
|
|
XM_011541121.3:c.15393T>C
|
XP_011539423.2:p.Leu5131=
|
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|
XM_017000822.2:c.15528T>C
|
XP_016856311.2:p.Leu5176=
|
|
|
XM_017000823.2:c.15501T>C
|
XP_016856312.2:p.Leu5167=
|
|
|
XM_017000824.2:c.15447T>C
|
XP_016856313.2:p.Leu5149=
|
|
|
XM_017000825.2:c.15432T>C
|
XP_016856314.2:p.Leu5144=
|
|
|
XM_017000826.2:c.15429T>C
|
XP_016856315.2:p.Leu5143=
|
|
|
XM_017000827.2:c.15414T>C
|
XP_016856316.2:p.Leu5138=
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|
XM_017000828.2:c.15390T>C
|
XP_016856317.2:p.Leu5130=
|
|
|
XM_017000829.2:c.15342T>C
|
XP_016856318.2:p.Leu5114=
|
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|
XM_017000830.2:c.15291T>C
|
XP_016856319.2:p.Leu5097=
|
|
|
NM_020765.3:c.15282T>C
MANE Select
|
NP_065816.2:p.Leu5094=
|
|
