ENST00000369538.4:c.1230G=
|
ENSP00000358551.4:p.Leu410=
|
|
ENST00000520113.7:c.1242G=
MANE Select
|
ENSP00000430075.3:p.Leu414=
|
|
ENST00000637080.1:c.1025G=
|
ENSP00000489753.1:n.1025G=
|
|
ENST00000639077.1:n.907G=
|
|
|
ENST00000369538.3:c.1329G=
|
ENSP00000358551.3:p.Leu443=
|
|
ENST00000520113.6:c.1341G=
|
ENSP00000430075.2:p.Leu447=
|
|
NM_000036.2:c.1341G=
|
NP_000027.2:p.Leu447=
|
|
NM_001172626.1:c.1329G=
|
NP_001166097.1:p.Leu443=
|
|
NM_000036.3:c.1242G=
MANE Select
|
NP_000027.3:p.Leu414=
|
|
NM_001172626.2:c.1230G=
|
NP_001166097.2:p.Leu410=
|
|