ENST00000455537.7:c.1077G>A
MANE Select
|
ENSP00000408979.2:p.Thr359=
|
|
ENST00000674619.1:c.1077G>A
|
ENSP00000502270.1:p.Thr359=
|
|
ENST00000675882.1:n.64G>A
|
|
|
ENST00000676081.1:n.223G>A
|
|
|
ENST00000676457.1:c.972G>A
|
ENSP00000501588.1:p.Thr324=
|
|
ENST00000286452.5:c.810G>A
|
ENSP00000286452.5:p.Thr270=
|
|
ENST00000455537.6:c.1077G>A
|
ENSP00000408979.2:p.Thr359=
|
|
NM_004984.2:c.1077G>A
|
NP_004975.2:p.Thr359=
|
|
NM_001354705.1:c.810G>A
|
NP_001341634.1:p.Thr270=
|
|
NM_004984.3:c.1077G>A
|
NP_004975.2:p.Thr359=
|
|
XR_002957324.1:n.1310G>A
|
|
|
NM_004984.4:c.1077G>A
MANE Select
|
NP_004975.2:p.Thr359=
|
|
NM_001354705.2:c.810G>A
|
NP_001341634.1:p.Thr270=
|
|