ENST00000345003.9:c.498A>T
MANE Select
|
ENSP00000340736.4:p.Ile166=
|
|
ENST00000296048.10:c.498A>T
|
ENSP00000296048.6:p.Ile166=
|
|
ENST00000345003.8:c.498A>T
|
ENSP00000340736.4:p.Ile166=
|
|
ENST00000461191.1:c.486A>T
|
ENSP00000420247.1:p.Ile162=
|
|
ENST00000469873.1:n.412A>T
|
|
|
ENST00000479119.1:n.114A>T
|
|
|
ENST00000483267.5:c.469+12400A>T
|
ENSP00000419499.1:n.469+12400A>T
|
|
ENST00000484197.5:c.498A>T
|
ENSP00000420683.1:p.Ile166=
|
|
ENST00000497528.5:n.137A>T
|
|
|
ENST00000627418.2:c.469+12400A>T
|
ENSP00000486061.1:n.469+12400A>T
|
|
NM_001184720.1:c.498A>T
|
NP_001171649.1:p.Ile166=
|
|
NM_001184721.1:c.498A>T
|
NP_001171650.1:p.Ile166=
|
|
NM_004130.3:c.498A>T
|
NP_004121.2:p.Ile166=
|
|
XM_017006275.1:c.321A>T
|
XP_016861764.1:p.Ile107=
|
|
XM_017006276.1:c.36A>T
|
XP_016861765.1:p.Ile12=
|
|
NM_004130.4:c.498A>T
MANE Select
|
NP_004121.2:p.Ile166=
|
|
NM_001184720.2:c.498A>T
|
NP_001171649.1:p.Ile166=
|
|
NM_001184721.2:c.498A>T
|
NP_001171650.1:p.Ile166=
|
|