ENST00000369538.4:c.532C>T
|
ENSP00000358551.4:p.Pro178Ser
|
|
ENST00000520113.7:c.544C>T
MANE Select
|
ENSP00000430075.3:p.Pro182Ser
|
|
ENST00000637080.1:c.547C>T
|
ENSP00000489753.1:p.Pro183Ser
|
|
ENST00000639077.1:n.209C>T
|
|
|
ENST00000369538.3:c.631C>T
|
ENSP00000358551.3:p.Pro211Ser
|
|
ENST00000485564.3:n.418C>T
|
|
|
ENST00000520113.6:c.643C>T
|
ENSP00000430075.2:p.Pro215Ser
|
|
NM_000036.2:c.643C>T
|
NP_000027.2:p.Pro215Ser
|
|
NM_001172626.1:c.631C>T
|
NP_001166097.1:p.Pro211Ser
|
|
NM_000036.3:c.544C>T
MANE Select
|
NP_000027.3:p.Pro182Ser
|
|
NM_001172626.2:c.532C>T
|
NP_001166097.2:p.Pro178Ser
|
|