ENST00000261304.7:c.752+194A>G
MANE Select
|
ENSP00000261304.2:n.752+194A>G
|
|
ENST00000261304.6:c.752+194A>G
|
ENSP00000261304.2:n.752+194A>G
|
|
ENST00000393568.8:c.683+194A>G
|
ENSP00000377198.4:n.683+194A>G
|
|
ENST00000393569.6:c.674+194A>G
|
ENSP00000377199.2:n.674+194A>G
|
|
ENST00000474294.6:n.742+194A>G
|
|
|
ENST00000477716.3:n.507+194A>G
|
|
|
ENST00000544807.6:c.584+194A>G
|
ENSP00000437513.2:n.584+194A>G
|
|
ENST00000555000.5:c.119+194A>G
|
ENSP00000450472.1:n.119+194A>G
|
|
ENST00000557316.5:c.*150+194A>G
|
ENSP00000452314.1:n.*150+194A>G
|
|
ENST00000622264.4:c.742+194A>G
|
|
|
NM_000153.3:c.752+194A>G
|
NP_000144.2:n.752+194A>G
|
|
NM_001201401.1:c.683+194A>G
|
NP_001188330.1:n.683+194A>G
|
|
NM_001201402.1:c.674+194A>G
|
NP_001188331.1:n.674+194A>G
|
|
XM_011536618.1:c.584+194A>G
|
XP_011534920.1:n.584+194A>G
|
|
XM_011536618.2:c.584+194A>G
|
XP_011534920.1:n.584+194A>G
|
|
NM_000153.4:c.752+194A>G
MANE Select
|
NP_000144.2:n.752+194A>G
|
|
NM_001201401.2:c.683+194A>G
|
NP_001188330.1:n.683+194A>G
|
|
NM_001201402.2:c.674+194A>G
|
NP_001188331.1:n.674+194A>G
|
|