ENST00000261304.7:c.697A>G
MANE Select
|
ENSP00000261304.2:p.Ile233Val
|
|
ENST00000261304.6:c.697A>G
|
ENSP00000261304.2:p.Ile233Val
|
|
ENST00000393568.8:c.628A>G
|
ENSP00000377198.4:p.Ile210Val
|
|
ENST00000393569.6:c.619A>G
|
ENSP00000377199.2:p.Ile207Val
|
|
ENST00000474294.6:n.687A>G
|
|
|
ENST00000477716.3:n.452A>G
|
|
|
ENST00000544807.6:c.529A>G
|
ENSP00000437513.2:p.Ile177Val
|
|
ENST00000554916.5:n.576A>G
|
|
|
ENST00000555000.5:c.64A>G
|
ENSP00000450472.1:p.Ile22Val
|
|
ENST00000557316.5:c.*95A>G
|
ENSP00000452314.1:n.*95A>G
|
|
ENST00000622264.4:c.687A>G
|
|
|
NM_000153.3:c.697A>G
|
NP_000144.2:p.Ile233Val
|
|
NM_001201401.1:c.628A>G
|
NP_001188330.1:p.Ile210Val
|
|
NM_001201402.1:c.619A>G
|
NP_001188331.1:p.Ile207Val
|
|
XM_011536618.1:c.529A>G
|
XP_011534920.1:p.Ile177Val
|
|
XM_011536618.2:c.529A>G
|
XP_011534920.1:p.Ile177Val
|
|
NM_000153.4:c.697A>G
MANE Select
|
NP_000144.2:p.Ile233Val
|
|
NM_001201401.2:c.628A>G
|
NP_001188330.1:p.Ile210Val
|
|
NM_001201402.2:c.619A>G
|
NP_001188331.1:p.Ile207Val
|
|