ENST00000217958.8:c.528A>G
MANE Select
|
ENSP00000217958.3:p.Leu176=
|
|
ENST00000217958.7:c.528A>G
|
ENSP00000217958.3:p.Leu176=
|
|
ENST00000340200.5:c.429A>G
|
ENSP00000345963.5:p.Leu143=
|
|
ENST00000361815.9:c.449A>G
|
ENSP00000354906.5:p.Asp150Gly
|
|
ENST00000372295.5:c.405A>G
|
ENSP00000361369.1:p.Leu135=
|
|
ENST00000372296.5:c.326A>G
|
ENSP00000361370.1:p.Asp109Gly
|
|
NM_002814.3:c.528A>G
|
NP_002805.1:p.Leu176=
|
|
NM_170750.2:c.449A>G
|
NP_736606.1:p.Asp150Gly
|
|
NM_002814.4:c.528A>G
MANE Select
|
NP_002805.1:p.Leu176=
|
|
NM_170750.3:c.449A>G
|
NP_736606.1:p.Asp150Gly
|
|