ENST00000369538.4:c.464C>A
|
ENSP00000358551.4:p.Pro155His
|
|
ENST00000520113.7:c.476C>A
MANE Select
|
ENSP00000430075.3:p.Pro159His
|
|
ENST00000637080.1:c.479C>A
|
ENSP00000489753.1:p.Pro160His
|
|
ENST00000639077.1:n.141C>A
|
|
|
ENST00000369538.3:c.563C>A
|
ENSP00000358551.3:p.Pro188His
|
|
ENST00000485564.3:n.350C>A
|
|
|
ENST00000520113.6:c.575C>A
|
ENSP00000430075.2:p.Pro192His
|
|
NM_000036.2:c.575C>A
|
NP_000027.2:p.Pro192His
|
|
NM_001172626.1:c.563C>A
|
NP_001166097.1:p.Pro188His
|
|
NM_000036.3:c.476C>A
MANE Select
|
NP_000027.3:p.Pro159His
|
|
NM_001172626.2:c.464C>A
|
NP_001166097.2:p.Pro155His
|
|