ENST00000432588.6:c.723G=
|
ENSP00000407473.2:p.Glu241=
|
|
ENST00000473257.3:c.594G=
|
ENSP00000501773.1:p.Glu198=
|
|
ENST00000477812.2:n.1270G=
|
|
|
ENST00000493945.6:c.723G=
|
ENSP00000494269.1:p.Glu241=
|
|
ENST00000642480.2:c.723G=
|
ENSP00000495995.2:p.Glu241=
|
|
ENST00000645576.1:c.675G=
|
ENSP00000496101.1:p.Glu225=
|
|
ENST00000646664.1:c.723G=
MANE Select
|
ENSP00000494750.1:p.Glu241=
|
|
ENST00000647275.1:c.357G=
|
ENSP00000494185.1:p.Glu119=
|
|
ENST00000674681.1:c.723G=
|
ENSP00000502821.1:p.Glu241=
|
|
ENST00000675515.1:c.723G=
|
ENSP00000501862.1:p.Glu241=
|
|
ENST00000676189.1:c.*266G=
|
ENSP00000502538.1:n.*266G=
|
|
ENST00000676319.1:c.88-577G=
|
ENSP00000502193.1:n.88-577G=
|
|
ENST00000676397.1:c.723G=
|
ENSP00000502286.1:p.Glu241=
|
|
ENST00000331789.9:c.723G=
|
ENSP00000349960.4:p.Glu241=
|
|
ENST00000425660.5:c.*386G=
|
ENSP00000409264.1:n.*386G=
|
|
ENST00000462494.5:n.1248G=
|
|
|
ENST00000473257.1:n.441G=
|
|
|
ENST00000484841.5:n.878G=
|
|
|
ENST00000493945.5:n.729G=
|
|
|
NM_001101.3:c.723G= , LRG_132t1:c.723G=
|
NP_001092.1:p.Glu241=
|
|
XM_006715764.1:c.357G=
|
XP_006715827.1:p.Glu119=
|
|
NM_001101.4:c.723G=
|
NP_001092.1:p.Glu241=
|
|
NM_001101.5:c.723G=
MANE Select
|
NP_001092.1:p.Glu241=
|
|