ENST00000496887.7:c.672C>T
|
ENSP00000434560.2:p.Thr224=
|
|
ENST00000646564.2:c.489C>T
|
ENSP00000495806.2:p.Thr163=
|
|
ENST00000155840.12:c.933C>T
MANE Select
|
ENSP00000155840.2:p.Thr311=
|
|
ENST00000335475.6:c.552C>T
|
ENSP00000334497.5:p.Thr184=
|
|
ENST00000646564.1:c.135C>T
|
ENSP00000495806.1:p.Thr45=
|
|
ENST00000155840.9:c.933C>T
|
ENSP00000155840.2:p.Thr311=
|
|
ENST00000335475.5:c.552C>T
|
ENSP00000334497.5:p.Thr184=
|
|
NM_000218.2:c.933C>T , LRG_287t1:c.933C>T
|
NP_000209.2:p.Thr311=
|
|
NM_181798.1:c.552C>T , LRG_287t2:c.552C>T
|
NP_861463.1:p.Thr184=
|
|
NM_000218.3:c.933C>T
MANE Select
|
NP_000209.2:p.Thr311=
|
|