ENST00000342695.9:c.996G>C
MANE Select
|
ENSP00000339182.4:p.Val332=
|
|
ENST00000295548.3:c.996G>C
|
ENSP00000295548.3:p.Val332=
|
|
ENST00000342695.8:c.996G>C
|
ENSP00000339182.4:p.Val332=
|
|
ENST00000392443.7:c.996G>C
|
ENSP00000376238.3:p.Val332=
|
|
ENST00000450950.6:c.*439G>C
|
ENSP00000402023.2:n.*439G>C
|
|
ENST00000490925.5:n.1104G>C
|
|
|
NM_032279.3:c.996G>C
|
NP_115655.2:p.Val332=
|
|
XM_005247829.2:c.996G>C
|
XP_005247886.1:p.Val332=
|
|
XM_011513232.1:c.996G>C
|
XP_011511534.1:p.Val332=
|
|
XR_241512.2:n.1297G>C
|
|
|
XR_924191.1:n.1297G>C
|
|
|
XM_011513232.2:c.996G>C
|
XP_011511534.1:p.Val332=
|
|
XM_017007318.1:c.669G>C
|
XP_016862807.1:p.Val223=
|
|
XM_017007319.1:c.996G>C
|
XP_016862808.1:p.Val332=
|
|
XR_001740324.2:n.1066G>C
|
|
|
XR_001740325.1:n.1066G>C
|
|
|
XR_002959602.1:n.1230G>C
|
|
|
XR_924191.3:n.1066G>C
|
|
|
NM_032279.4:c.996G>C
MANE Select
|
NP_115655.2:p.Val332=
|
|