ENST00000216075.11:c.825T>C
MANE Select
|
ENSP00000216075.6:p.Ile275=
|
|
ENST00000216075.10:c.825T>C
|
ENSP00000216075.6:p.Ile275=
|
|
ENST00000395732.7:c.811T>C
|
ENSP00000379081.3:p.Ter271Arg
|
|
ENST00000395733.7:c.694T>C
|
ENSP00000379082.3:p.Ter232Arg
|
|
ENST00000451761.1:c.765T>C
|
ENSP00000409894.1:p.Ile255=
|
|
NM_017584.5:c.825T>C
|
NP_060054.4:p.Ile275=
|
|
XM_005261925.3:c.687T>C
|
XP_005261982.1:p.Ile229=
|
|
XR_244455.2:n.3321T>C
|
|
|
XM_005261925.4:c.687T>C
|
XP_005261982.1:p.Ile229=
|
|
NM_017584.6:c.825T>C
MANE Select
|
NP_060054.4:p.Ile275=
|
|