ENST00000369538.4:c.395T>C
|
ENSP00000358551.4:p.Val132Ala
|
|
ENST00000520113.7:c.407T>C
MANE Select
|
ENSP00000430075.3:p.Val136Ala
|
|
ENST00000637080.1:c.410T>C
|
ENSP00000489753.1:p.Val137Ala
|
|
ENST00000639077.1:n.72T>C
|
|
|
ENST00000369538.3:c.494T>C
|
ENSP00000358551.3:p.Val165Ala
|
|
ENST00000485564.3:n.281T>C
|
|
|
ENST00000520113.6:c.506T>C
|
ENSP00000430075.2:p.Val169Ala
|
|
NM_000036.2:c.506T>C
|
NP_000027.2:p.Val169Ala
|
|
NM_001172626.1:c.494T>C
|
NP_001166097.1:p.Val165Ala
|
|
NM_000036.3:c.407T>C
MANE Select
|
NP_000027.3:p.Val136Ala
|
|
NM_001172626.2:c.395T>C
|
NP_001166097.2:p.Val132Ala
|
|