ENST00000369538.4:c.534A>T
|
ENSP00000358551.4:p.Pro178=
|
|
ENST00000520113.7:c.546A>T
MANE Select
|
ENSP00000430075.3:p.Pro182=
|
|
ENST00000637080.1:c.549A>T
|
ENSP00000489753.1:p.Pro183=
|
|
ENST00000639077.1:n.211A>T
|
|
|
ENST00000369538.3:c.633A>T
|
ENSP00000358551.3:p.Pro211=
|
|
ENST00000485564.3:n.420A>T
|
|
|
ENST00000520113.6:c.645A>T
|
ENSP00000430075.2:p.Pro215=
|
|
NM_000036.2:c.645A>T
|
NP_000027.2:p.Pro215=
|
|
NM_001172626.1:c.633A>T
|
NP_001166097.1:p.Pro211=
|
|
NM_000036.3:c.546A>T
MANE Select
|
NP_000027.3:p.Pro182=
|
|
NM_001172626.2:c.534A>T
|
NP_001166097.2:p.Pro178=
|
|