ENST00000369538.4:c.1266G>C
|
ENSP00000358551.4:p.Leu422=
|
|
ENST00000520113.7:c.1278G>C
MANE Select
|
ENSP00000430075.3:p.Leu426=
|
|
ENST00000637080.1:c.1061G>C
|
ENSP00000489753.1:n.1061G>C
|
|
ENST00000639077.1:n.943G>C
|
|
|
ENST00000369538.3:c.1365G>C
|
ENSP00000358551.3:p.Leu455=
|
|
ENST00000520113.6:c.1377G>C
|
ENSP00000430075.2:p.Leu459=
|
|
NM_000036.2:c.1377G>C
|
NP_000027.2:p.Leu459=
|
|
NM_001172626.1:c.1365G>C
|
NP_001166097.1:p.Leu455=
|
|
NM_000036.3:c.1278G>C
MANE Select
|
NP_000027.3:p.Leu426=
|
|
NM_001172626.2:c.1266G>C
|
NP_001166097.2:p.Leu422=
|
|