ENST00000260191.8:c.499C>G
MANE Select
|
ENSP00000260191.2:p.Gln167Glu
|
|
ENST00000260191.7:c.499C>G
|
ENSP00000260191.2:p.Gln167Glu
|
|
ENST00000260191.6:c.499C>G
|
ENSP00000260191.2:p.Gln167Glu
|
|
ENST00000537778.5:c.466C>G
|
ENSP00000443118.1:p.Gln156Glu
|
|
ENST00000543092.1:c.285C>G
|
|
|
NM_006028.4:c.499C>G
|
NP_006019.1:p.Gln167Glu
|
|
XM_011543063.1:c.466C>G
|
XP_011541365.1:p.Gln156Glu
|
|
XM_011543064.1:c.298C>G
|
XP_011541366.1:p.Gln100Glu
|
|
XM_011543065.1:c.292C>G
|
XP_011541367.1:p.Gln98Glu
|
|
XM_011543066.1:c.466C>G
|
XP_011541368.1:p.Gln156Glu
|
|
NM_001363563.1:c.466C>G
|
NP_001350492.1:p.Gln156Glu
|
|
XM_017018552.2:c.292C>G
|
XP_016874041.1:p.Gln98Glu
|
|
XM_024448767.1:c.205C>G
|
XP_024304535.1:p.Gln69Glu
|
|
XR_001748034.2:n.750C>G
|
|
|
NM_001363563.2:c.466C>G
|
NP_001350492.1:p.Gln156Glu
|
|
NM_006028.5:c.499C>G
MANE Select
|
NP_006019.1:p.Gln167Glu
|
|