ENST00000261304.7:c.654C>G
MANE Select
|
ENSP00000261304.2:p.Leu218=
|
|
ENST00000261304.6:c.654C>G
|
ENSP00000261304.2:p.Leu218=
|
|
ENST00000393568.8:c.585C>G
|
ENSP00000377198.4:p.Leu195=
|
|
ENST00000393569.6:c.576C>G
|
ENSP00000377199.2:p.Leu192=
|
|
ENST00000474294.6:n.644C>G
|
|
|
ENST00000477716.3:n.409C>G
|
|
|
ENST00000544807.6:c.486C>G
|
ENSP00000437513.2:p.Leu162=
|
|
ENST00000554916.5:n.533C>G
|
|
|
ENST00000555000.5:c.21C>G
|
ENSP00000450472.1:p.Leu7=
|
|
ENST00000557316.5:c.*52C>G
|
ENSP00000452314.1:n.*52C>G
|
|
ENST00000622264.4:c.644C>G
|
|
|
NM_000153.3:c.654C>G
|
NP_000144.2:p.Leu218=
|
|
NM_001201401.1:c.585C>G
|
NP_001188330.1:p.Leu195=
|
|
NM_001201402.1:c.576C>G
|
NP_001188331.1:p.Leu192=
|
|
XM_011536618.1:c.486C>G
|
XP_011534920.1:p.Leu162=
|
|
XM_011536618.2:c.486C>G
|
XP_011534920.1:p.Leu162=
|
|
NM_000153.4:c.654C>G
MANE Select
|
NP_000144.2:p.Leu218=
|
|
NM_001201401.2:c.585C>G
|
NP_001188330.1:p.Leu195=
|
|
NM_001201402.2:c.576C>G
|
NP_001188331.1:p.Leu192=
|
|