ENST00000430710.8:c.287T=
|
ENSP00000406288.3:p.Leu96=
|
|
ENST00000553651.2:n.2930T=
|
|
|
ENST00000555962.6:c.-111+2756T=
|
ENSP00000495174.1:n.-111+2756T=
|
|
ENST00000557364.6:c.1124T=
|
ENSP00000451601.1:p.Leu375=
|
|
ENST00000642518.1:c.287T=
|
ENSP00000496722.1:p.Leu96=
|
|
ENST00000643048.1:n.1419T=
|
|
|
ENST00000643469.1:c.1124T=
|
ENSP00000495070.1:p.Leu375=
|
|
ENST00000645140.1:c.1036T=
|
|
|
ENST00000645929.1:c.287T=
|
ENSP00000494402.1:p.Leu96=
|
|
ENST00000646063.1:c.1211T=
|
ENSP00000496565.1:p.Leu404=
|
|
ENST00000646340.1:c.1130T=
|
ENSP00000496730.1:p.Leu377=
|
|
ENST00000646647.2:c.1124T=
MANE Select
|
ENSP00000495240.1:p.Leu375=
|
|
ENST00000399982.6:c.1124T=
|
ENSP00000382863.2:p.Leu375=
|
|
ENST00000430710.7:c.287T=
|
ENSP00000406288.3:p.Leu96=
|
|
ENST00000555962.5:n.150+2756T=
|
|
|
ENST00000557364.5:c.1124T=
|
ENSP00000451601.1:p.Leu375=
|
|
NM_001170629.1:c.1124T=
|
NP_001164100.1:p.Leu375=
|
|
NM_020920.3:c.287T=
|
NP_065971.2:p.Leu96=
|
|
NM_001170629.2:c.1124T=
MANE Select
|
NP_001164100.1:p.Leu375=
|
|
NM_020920.4:c.287T=
|
NP_065971.2:p.Leu96=
|
|