ENST00000369538.4:c.489G>T
|
ENSP00000358551.4:p.Arg163=
|
|
ENST00000520113.7:c.501G>T
MANE Select
|
ENSP00000430075.3:p.Arg167=
|
|
ENST00000637080.1:c.504G>T
|
ENSP00000489753.1:p.Arg168=
|
|
ENST00000639077.1:n.166G>T
|
|
|
ENST00000369538.3:c.588G>T
|
ENSP00000358551.3:p.Arg196=
|
|
ENST00000485564.3:n.375G>T
|
|
|
ENST00000520113.6:c.600G>T
|
ENSP00000430075.2:p.Arg200=
|
|
NM_000036.2:c.600G>T
|
NP_000027.2:p.Arg200=
|
|
NM_001172626.1:c.588G>T
|
NP_001166097.1:p.Arg196=
|
|
NM_000036.3:c.501G>T
MANE Select
|
NP_000027.3:p.Arg167=
|
|
NM_001172626.2:c.489G>T
|
NP_001166097.2:p.Arg163=
|
|