ENST00000455537.7:c.796A>T
MANE Select
|
ENSP00000408979.2:p.Ile266Phe
|
|
ENST00000674619.1:c.796A>T
|
ENSP00000502270.1:p.Ile266Phe
|
|
ENST00000676457.1:c.691A>T
|
ENSP00000501588.1:p.Ile231Phe
|
|
ENST00000286452.5:c.529A>T
|
ENSP00000286452.5:p.Ile177Phe
|
|
ENST00000455537.6:c.796A>T
|
ENSP00000408979.2:p.Ile266Phe
|
|
NM_004984.2:c.796A>T
|
NP_004975.2:p.Ile266Phe
|
|
NM_001354705.1:c.529A>T
|
NP_001341634.1:p.Ile177Phe
|
|
NM_004984.3:c.796A>T
|
NP_004975.2:p.Ile266Phe
|
|
XR_002957324.1:n.1029A>T
|
|
|
NM_004984.4:c.796A>T
MANE Select
|
NP_004975.2:p.Ile266Phe
|
|
NM_001354705.2:c.529A>T
|
NP_001341634.1:p.Ile177Phe
|
|