ENST00000263038.9:c.747G>T
MANE Select
|
ENSP00000263038.4:p.Val249=
|
|
ENST00000263038.8:c.747G>T
|
ENSP00000263038.4:p.Val249=
|
|
ENST00000396913.6:c.447G>T
|
ENSP00000380121.2:p.Val149=
|
|
ENST00000396920.7:c.696G>T
|
ENSP00000380126.3:p.Val232=
|
|
ENST00000453759.6:c.447G>T
|
ENSP00000412525.2:p.Val149=
|
|
NM_001037537.1:c.447G>T
|
NP_001032626.1:p.Val149=
|
|
NM_006214.3:c.747G>T
|
NP_006205.1:p.Val249=
|
|
XM_005252469.2:c.528G>T
|
XP_005252526.1:p.Val176=
|
|
NM_001323080.1:c.447G>T
|
NP_001310009.1:p.Val149=
|
|
NM_001323082.1:c.753G>T
|
NP_001310011.1:p.Val251=
|
|
NM_001323083.1:c.483G>T
|
NP_001310012.1:p.Val161=
|
|
NM_001323084.1:c.453G>T
|
NP_001310013.1:p.Val151=
|
|
NM_006214.4:c.747G>T
MANE Select
|
NP_006205.1:p.Val249=
|
|
NM_001037537.2:c.447G>T
|
NP_001032626.1:p.Val149=
|
|
NM_001323080.2:c.447G>T
|
NP_001310009.1:p.Val149=
|
|
NM_001323082.2:c.753G>T
|
NP_001310011.1:p.Val251=
|
|
NM_001323083.2:c.483G>T
|
NP_001310012.1:p.Val161=
|
|
NM_001323084.2:c.453G>T
|
NP_001310013.1:p.Val151=
|
|