ENST00000369538.4:c.456G>C
|
ENSP00000358551.4:p.Gln152His
|
|
ENST00000520113.7:c.468G>C
MANE Select
|
ENSP00000430075.3:p.Gln156His
|
|
ENST00000637080.1:c.471G>C
|
ENSP00000489753.1:p.Gln157His
|
|
ENST00000639077.1:n.133G>C
|
|
|
ENST00000369538.3:c.555G>C
|
ENSP00000358551.3:p.Gln185His
|
|
ENST00000485564.3:n.342G>C
|
|
|
ENST00000520113.6:c.567G>C
|
ENSP00000430075.2:p.Gln189His
|
|
NM_000036.2:c.567G>C
|
NP_000027.2:p.Gln189His
|
|
NM_001172626.1:c.555G>C
|
NP_001166097.1:p.Gln185His
|
|
NM_000036.3:c.468G>C
MANE Select
|
NP_000027.3:p.Gln156His
|
|
NM_001172626.2:c.456G>C
|
NP_001166097.2:p.Gln152His
|
|