ENST00000496887.7:c.1180A=
|
ENSP00000434560.2:p.Thr394=
|
|
ENST00000646564.2:c.997A=
|
ENSP00000495806.2:p.Thr333=
|
|
ENST00000155840.12:c.1537A=
MANE Select
|
ENSP00000155840.2:p.Thr513=
|
|
ENST00000335475.6:c.1156A=
|
ENSP00000334497.5:p.Thr386=
|
|
ENST00000646564.1:c.643A=
|
ENSP00000495806.1:p.Thr215=
|
|
ENST00000155840.9:c.1537A=
|
ENSP00000155840.2:p.Thr513=
|
|
ENST00000335475.5:c.1156A=
|
ENSP00000334497.5:p.Thr386=
|
|
NM_000218.2:c.1537A= , LRG_287t1:c.1537A=
|
NP_000209.2:p.Thr513=
|
|
NM_181798.1:c.1156A= , LRG_287t2:c.1156A=
|
NP_861463.1:p.Thr386=
|
|
NM_000218.3:c.1537A=
MANE Select
|
NP_000209.2:p.Thr513=
|
|