ENST00000496887.7:c.714G>T
|
ENSP00000434560.2:p.Gly238=
|
|
ENST00000646564.2:c.531G>T
|
ENSP00000495806.2:p.Gly177=
|
|
ENST00000155840.12:c.975G>T
MANE Select
|
ENSP00000155840.2:p.Gly325=
|
|
ENST00000335475.6:c.594G>T
|
ENSP00000334497.5:p.Gly198=
|
|
ENST00000646564.1:c.177G>T
|
ENSP00000495806.1:p.Gly59=
|
|
ENST00000155840.9:c.975G>T
|
ENSP00000155840.2:p.Gly325=
|
|
ENST00000335475.5:c.594G>T
|
ENSP00000334497.5:p.Gly198=
|
|
NM_000218.2:c.975G>T , LRG_287t1:c.975G>T
|
NP_000209.2:p.Gly325=
|
|
NM_181798.1:c.594G>T , LRG_287t2:c.594G>T
|
NP_861463.1:p.Gly198=
|
|
NM_000218.3:c.975G>T
MANE Select
|
NP_000209.2:p.Gly325=
|
|