ENST00000455537.7:c.510T>G
MANE Select
|
ENSP00000408979.2:p.Thr170=
|
|
ENST00000674619.1:c.510T>G
|
ENSP00000502270.1:p.Thr170=
|
|
ENST00000676457.1:c.405T>G
|
ENSP00000501588.1:p.Thr135=
|
|
ENST00000286452.5:c.243T>G
|
ENSP00000286452.5:p.Thr81=
|
|
ENST00000455537.6:c.510T>G
|
ENSP00000408979.2:p.Thr170=
|
|
NM_004984.2:c.510T>G
|
NP_004975.2:p.Thr170=
|
|
NM_001354705.1:c.243T>G
|
NP_001341634.1:p.Thr81=
|
|
NM_004984.3:c.510T>G
|
NP_004975.2:p.Thr170=
|
|
XR_002957324.1:n.743T>G
|
|
|
NM_004984.4:c.510T>G
MANE Select
|
NP_004975.2:p.Thr170=
|
|
NM_001354705.2:c.243T>G
|
NP_001341634.1:p.Thr81=
|
|