ENST00000264094.8:c.1929G>A
MANE Select
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ENSP00000264094.3:p.Glu643=
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ENST00000264094.7:c.1929G>A
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ENSP00000264094.3:p.Glu643=
|
|
ENST00000393937.6:c.1494G>A
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ENSP00000377512.2:p.Glu498=
|
|
ENST00000409249.5:c.1094-90G>A
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ENSP00000387103.1:n.1094-90G>A
|
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ENST00000409549.5:c.1761G>A
|
ENSP00000386696.1:p.Glu587=
|
|
ENST00000409986.5:c.1494G>A
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ENSP00000386545.1:p.Glu498=
|
|
ENST00000470907.6:n.1312G>A
|
|
|
NM_001289164.1:c.1494G>A
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NP_001276093.1:p.Glu498=
|
|
NM_001289165.1:c.846G>A
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NP_001276094.1:p.Glu282=
|
|
NM_032603.3:c.1929G>A
|
NP_115992.1:p.Glu643=
|
|
XM_011533134.1:c.1929G>A
|
XP_011531436.1:p.Glu643=
|
|
NM_001289164.2:c.1494G>A
|
NP_001276093.1:p.Glu498=
|
|
NM_032603.4:c.1929G>A
|
NP_115992.1:p.Glu643=
|
|
XM_011533134.2:c.1929G>A
|
XP_011531436.1:p.Glu643=
|
|
XM_017005112.1:c.846G>A
|
XP_016860601.1:p.Glu282=
|
|
XM_024453176.1:c.1929G>A
|
XP_024308944.1:p.Glu643=
|
|
XM_024453177.1:c.1929G>A
|
XP_024308945.1:p.Glu643=
|
|
XM_024453178.1:c.1929G>A
|
XP_024308946.1:p.Glu643=
|
|
NM_032603.5:c.1929G>A
MANE Select
|
NP_115992.1:p.Glu643=
|
|
NM_001289164.3:c.1494G>A
|
NP_001276093.1:p.Glu498=
|
|
NM_001289165.2:c.846G>A
|
NP_001276094.1:p.Glu282=
|
|