ENST00000216075.11:c.824T>C
MANE Select
|
ENSP00000216075.6:p.Ile275Thr
|
|
ENST00000216075.10:c.824T>C
|
ENSP00000216075.6:p.Ile275Thr
|
|
ENST00000395732.7:c.810T>C
|
ENSP00000379081.3:p.His270=
|
|
ENST00000395733.7:c.693T>C
|
ENSP00000379082.3:p.His231=
|
|
ENST00000451761.1:c.764T>C
|
ENSP00000409894.1:p.Ile255Thr
|
|
NM_017584.5:c.824T>C
|
NP_060054.4:p.Ile275Thr
|
|
XM_005261925.3:c.686T>C
|
XP_005261982.1:p.Ile229Thr
|
|
XR_244455.2:n.3320T>C
|
|
|
XM_005261925.4:c.686T>C
|
XP_005261982.1:p.Ile229Thr
|
|
NM_017584.6:c.824T>C
MANE Select
|
NP_060054.4:p.Ile275Thr
|
|