ENST00000369538.4:c.512T>A
|
ENSP00000358551.4:p.Val171Glu
|
|
ENST00000520113.7:c.524T>A
MANE Select
|
ENSP00000430075.3:p.Val175Glu
|
|
ENST00000637080.1:c.527T>A
|
ENSP00000489753.1:p.Val176Glu
|
|
ENST00000639077.1:n.189T>A
|
|
|
ENST00000369538.3:c.611T>A
|
ENSP00000358551.3:p.Val204Glu
|
|
ENST00000485564.3:n.398T>A
|
|
|
ENST00000520113.6:c.623T>A
|
ENSP00000430075.2:p.Val208Glu
|
|
NM_000036.2:c.623T>A
|
NP_000027.2:p.Val208Glu
|
|
NM_001172626.1:c.611T>A
|
NP_001166097.1:p.Val204Glu
|
|
NM_000036.3:c.524T>A
MANE Select
|
NP_000027.3:p.Val175Glu
|
|
NM_001172626.2:c.512T>A
|
NP_001166097.2:p.Val171Glu
|
|