ENST00000260191.8:c.483T>C
MANE Select
|
ENSP00000260191.2:p.Ala161=
|
|
ENST00000260191.7:c.483T>C
|
ENSP00000260191.2:p.Ala161=
|
|
ENST00000260191.6:c.483T>C
|
ENSP00000260191.2:p.Ala161=
|
|
ENST00000537778.5:c.450T>C
|
ENSP00000443118.1:p.Ala150=
|
|
ENST00000543092.1:c.269T>C
|
|
|
NM_006028.4:c.483T>C
|
NP_006019.1:p.Ala161=
|
|
XM_011543063.1:c.450T>C
|
XP_011541365.1:p.Ala150=
|
|
XM_011543064.1:c.282T>C
|
XP_011541366.1:p.Ala94=
|
|
XM_011543065.1:c.276T>C
|
XP_011541367.1:p.Ala92=
|
|
XM_011543066.1:c.450T>C
|
XP_011541368.1:p.Ala150=
|
|
NM_001363563.1:c.450T>C
|
NP_001350492.1:p.Ala150=
|
|
XM_017018552.2:c.276T>C
|
XP_016874041.1:p.Ala92=
|
|
XM_024448767.1:c.189T>C
|
XP_024304535.1:p.Ala63=
|
|
XR_001748034.2:n.734T>C
|
|
|
NM_001363563.2:c.450T>C
|
NP_001350492.1:p.Ala150=
|
|
NM_006028.5:c.483T>C
MANE Select
|
NP_006019.1:p.Ala161=
|
|