ENST00000369538.4:c.1256A>C
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ENSP00000358551.4:p.Glu419Ala
|
|
ENST00000520113.7:c.1268A>C
MANE Select
|
ENSP00000430075.3:p.Glu423Ala
|
|
ENST00000637080.1:c.1051A>C
|
ENSP00000489753.1:n.1051A>C
|
|
ENST00000639077.1:n.933A>C
|
|
|
ENST00000369538.3:c.1355A>C
|
ENSP00000358551.3:p.Glu452Ala
|
|
ENST00000520113.6:c.1367A>C
|
ENSP00000430075.2:p.Glu456Ala
|
|
NM_000036.2:c.1367A>C
|
NP_000027.2:p.Glu456Ala
|
|
NM_001172626.1:c.1355A>C
|
NP_001166097.1:p.Glu452Ala
|
|
NM_000036.3:c.1268A>C
MANE Select
|
NP_000027.3:p.Glu423Ala
|
|
NM_001172626.2:c.1256A>C
|
NP_001166097.2:p.Glu419Ala
|
|