ENST00000430710.8:c.109T>C
|
ENSP00000406288.3:p.Leu37=
|
|
ENST00000553651.2:n.2752T>C
|
|
|
ENST00000555962.6:c.-111+2578T>C
|
ENSP00000495174.1:n.-111+2578T>C
|
|
ENST00000557364.6:c.946T>C
|
ENSP00000451601.1:p.Leu316=
|
|
ENST00000642518.1:c.109T>C
|
ENSP00000496722.1:p.Leu37=
|
|
ENST00000643048.1:n.1241T>C
|
|
|
ENST00000643469.1:c.946T>C
|
ENSP00000495070.1:p.Leu316=
|
|
ENST00000645140.1:c.858T>C
|
|
|
ENST00000645929.1:c.109T>C
|
ENSP00000494402.1:p.Leu37=
|
|
ENST00000646063.1:c.1033T>C
|
ENSP00000496565.1:p.Leu345=
|
|
ENST00000646340.1:c.952T>C
|
ENSP00000496730.1:p.Leu318=
|
|
ENST00000646647.2:c.946T>C
MANE Select
|
ENSP00000495240.1:p.Leu316=
|
|
ENST00000399982.6:c.946T>C
|
ENSP00000382863.2:p.Leu316=
|
|
ENST00000430710.7:c.109T>C
|
ENSP00000406288.3:p.Leu37=
|
|
ENST00000553283.1:c.199T>C
|
ENSP00000450860.1:p.Leu67=
|
|
ENST00000555962.5:n.150+2578T>C
|
|
|
ENST00000557364.5:c.946T>C
|
ENSP00000451601.1:p.Leu316=
|
|
NM_001170629.1:c.946T>C
|
NP_001164100.1:p.Leu316=
|
|
NM_020920.3:c.109T>C
|
NP_065971.2:p.Leu37=
|
|
NM_001170629.2:c.946T>C
MANE Select
|
NP_001164100.1:p.Leu316=
|
|
NM_020920.4:c.109T>C
|
NP_065971.2:p.Leu37=
|
|