ENST00000263038.9:c.737T>C
MANE Select
|
ENSP00000263038.4:p.Val246Ala
|
|
ENST00000263038.8:c.737T>C
|
ENSP00000263038.4:p.Val246Ala
|
|
ENST00000396913.6:c.437T>C
|
ENSP00000380121.2:p.Val146Ala
|
|
ENST00000396920.7:c.686T>C
|
ENSP00000380126.3:p.Val229Ala
|
|
ENST00000453759.6:c.437T>C
|
ENSP00000412525.2:p.Val146Ala
|
|
NM_001037537.1:c.437T>C
|
NP_001032626.1:p.Val146Ala
|
|
NM_006214.3:c.737T>C
|
NP_006205.1:p.Val246Ala
|
|
XM_005252469.2:c.518T>C
|
XP_005252526.1:p.Val173Ala
|
|
NM_001323080.1:c.437T>C
|
NP_001310009.1:p.Val146Ala
|
|
NM_001323082.1:c.743T>C
|
NP_001310011.1:p.Val248Ala
|
|
NM_001323083.1:c.473T>C
|
NP_001310012.1:p.Val158Ala
|
|
NM_001323084.1:c.443T>C
|
NP_001310013.1:p.Val148Ala
|
|
NM_006214.4:c.737T>C
MANE Select
|
NP_006205.1:p.Val246Ala
|
|
NM_001037537.2:c.437T>C
|
NP_001032626.1:p.Val146Ala
|
|
NM_001323080.2:c.437T>C
|
NP_001310009.1:p.Val146Ala
|
|
NM_001323082.2:c.743T>C
|
NP_001310011.1:p.Val248Ala
|
|
NM_001323083.2:c.473T>C
|
NP_001310012.1:p.Val158Ala
|
|
NM_001323084.2:c.443T>C
|
NP_001310013.1:p.Val148Ala
|
|