ENST00000216075.11:c.823A>G
MANE Select
|
ENSP00000216075.6:p.Ile275Val
|
|
ENST00000216075.10:c.823A>G
|
ENSP00000216075.6:p.Ile275Val
|
|
ENST00000395732.7:c.809A>G
|
ENSP00000379081.3:p.His270Arg
|
|
ENST00000395733.7:c.692A>G
|
ENSP00000379082.3:p.His231Arg
|
|
ENST00000451761.1:c.763A>G
|
ENSP00000409894.1:p.Ile255Val
|
|
NM_017584.5:c.823A>G
|
NP_060054.4:p.Ile275Val
|
|
XM_005261925.3:c.685A>G
|
XP_005261982.1:p.Ile229Val
|
|
XR_244455.2:n.3319A>G
|
|
|
XM_005261925.4:c.685A>G
|
XP_005261982.1:p.Ile229Val
|
|
NM_017584.6:c.823A>G
MANE Select
|
NP_060054.4:p.Ile275Val
|
|