ENST00000369538.4:c.371T>C
|
ENSP00000358551.4:p.Val124Ala
|
|
ENST00000520113.7:c.383T>C
MANE Select
|
ENSP00000430075.3:p.Val128Ala
|
|
ENST00000637080.1:c.386T>C
|
ENSP00000489753.1:p.Val129Ala
|
|
ENST00000639077.1:n.48T>C
|
|
|
ENST00000369538.3:c.470T>C
|
ENSP00000358551.3:p.Val157Ala
|
|
ENST00000485564.3:n.257T>C
|
|
|
ENST00000520113.6:c.482T>C
|
ENSP00000430075.2:p.Val161Ala
|
|
NM_000036.2:c.482T>C
|
NP_000027.2:p.Val161Ala
|
|
NM_001172626.1:c.470T>C
|
NP_001166097.1:p.Val157Ala
|
|
NM_000036.3:c.383T>C
MANE Select
|
NP_000027.3:p.Val128Ala
|
|
NM_001172626.2:c.371T>C
|
NP_001166097.2:p.Val124Ala
|
|