ENST00000261304.7:c.747T>G
MANE Select
|
ENSP00000261304.2:p.Val249=
|
|
ENST00000261304.6:c.747T>G
|
ENSP00000261304.2:p.Val249=
|
|
ENST00000393568.8:c.678T>G
|
ENSP00000377198.4:p.Val226=
|
|
ENST00000393569.6:c.669T>G
|
ENSP00000377199.2:p.Val223=
|
|
ENST00000474294.6:n.737T>G
|
|
|
ENST00000477716.3:n.502T>G
|
|
|
ENST00000544807.6:c.579T>G
|
ENSP00000437513.2:p.Val193=
|
|
ENST00000554916.5:n.626T>G
|
|
|
ENST00000555000.5:c.114T>G
|
ENSP00000450472.1:p.Val38=
|
|
ENST00000557316.5:c.*145T>G
|
ENSP00000452314.1:n.*145T>G
|
|
ENST00000622264.4:c.737T>G
|
|
|
NM_000153.3:c.747T>G
|
NP_000144.2:p.Val249=
|
|
NM_001201401.1:c.678T>G
|
NP_001188330.1:p.Val226=
|
|
NM_001201402.1:c.669T>G
|
NP_001188331.1:p.Val223=
|
|
XM_011536618.1:c.579T>G
|
XP_011534920.1:p.Val193=
|
|
XM_011536618.2:c.579T>G
|
XP_011534920.1:p.Val193=
|
|
NM_000153.4:c.747T>G
MANE Select
|
NP_000144.2:p.Val249=
|
|
NM_001201401.2:c.678T>G
|
NP_001188330.1:p.Val226=
|
|
NM_001201402.2:c.669T>G
|
NP_001188331.1:p.Val223=
|
|