ENST00000260191.8:c.473A>C
MANE Select
|
ENSP00000260191.2:p.Glu158Ala
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ENST00000260191.7:c.473A>C
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ENSP00000260191.2:p.Glu158Ala
|
|
ENST00000260191.6:c.473A>C
|
ENSP00000260191.2:p.Glu158Ala
|
|
ENST00000537778.5:c.440A>C
|
ENSP00000443118.1:p.Glu147Ala
|
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ENST00000543092.1:c.259A>C
|
|
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NM_006028.4:c.473A>C
|
NP_006019.1:p.Glu158Ala
|
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XM_011543063.1:c.440A>C
|
XP_011541365.1:p.Glu147Ala
|
|
XM_011543064.1:c.272A>C
|
XP_011541366.1:p.Glu91Ala
|
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XM_011543065.1:c.266A>C
|
XP_011541367.1:p.Glu89Ala
|
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XM_011543066.1:c.440A>C
|
XP_011541368.1:p.Glu147Ala
|
|
NM_001363563.1:c.440A>C
|
NP_001350492.1:p.Glu147Ala
|
|
XM_017018552.2:c.266A>C
|
XP_016874041.1:p.Glu89Ala
|
|
XM_024448767.1:c.179A>C
|
XP_024304535.1:p.Glu60Ala
|
|
XR_001748034.2:n.724A>C
|
|
|
NM_001363563.2:c.440A>C
|
NP_001350492.1:p.Glu147Ala
|
|
NM_006028.5:c.473A>C
MANE Select
|
NP_006019.1:p.Glu158Ala
|
|