ENST00000260191.8:c.467G=
MANE Select
|
ENSP00000260191.2:p.Ser156=
|
|
ENST00000260191.7:c.467G=
|
ENSP00000260191.2:p.Ser156=
|
|
ENST00000260191.6:c.467G=
|
ENSP00000260191.2:p.Ser156=
|
|
ENST00000537778.5:c.434G=
|
ENSP00000443118.1:p.Ser145=
|
|
ENST00000543092.1:c.253G=
|
|
|
NM_006028.4:c.467G=
|
NP_006019.1:p.Ser156=
|
|
XM_011543063.1:c.434G=
|
XP_011541365.1:p.Ser145=
|
|
XM_011543064.1:c.266G=
|
XP_011541366.1:p.Ser89=
|
|
XM_011543065.1:c.260G=
|
XP_011541367.1:p.Ser87=
|
|
XM_011543066.1:c.434G=
|
XP_011541368.1:p.Ser145=
|
|
NM_001363563.1:c.434G=
|
NP_001350492.1:p.Ser145=
|
|
XM_017018552.2:c.260G=
|
XP_016874041.1:p.Ser87=
|
|
XM_024448767.1:c.173G=
|
XP_024304535.1:p.Ser58=
|
|
XR_001748034.2:n.718G=
|
|
|
NM_001363563.2:c.434G=
|
NP_001350492.1:p.Ser145=
|
|
NM_006028.5:c.467G=
MANE Select
|
NP_006019.1:p.Ser156=
|
|