ENST00000696136.1:c.369G>A
|
ENSP00000512428.1:p.Leu123=
|
|
ENST00000696137.1:c.336G>A
|
ENSP00000512429.1:p.Leu112=
|
|
ENST00000696152.1:c.336G>A
|
ENSP00000512443.1:p.Leu112=
|
|
ENST00000696228.1:c.369G>A
|
ENSP00000512494.1:p.Leu123=
|
|
ENST00000241393.4:c.381G>A
MANE Select
|
ENSP00000241393.3:p.Leu127=
|
|
ENST00000241393.3:c.381G>A
|
ENSP00000241393.3:p.Leu127=
|
|
ENST00000409817.1:c.393G>A
|
ENSP00000386884.1:p.Leu131=
|
|
ENST00000466288.1:n.575G>A
|
|
|
NM_001008540.1:c.393G>A
|
NP_001008540.1:p.Leu131=
|
|
NM_003467.2:c.381G>A , LRG_51t1:c.381G>A
|
NP_003458.1:p.Leu127=
|
|
NM_001008540.2:c.393G>A
|
NP_001008540.1:p.Leu131=
|
|
NM_001348056.1:c.594G>A
|
NP_001334985.1:p.Leu198=
|
|
NM_001348059.1:c.480G>A
|
NP_001334988.1:p.Leu160=
|
|
NM_001348060.1:c.336G>A
|
NP_001334989.1:p.Leu112=
|
|
NM_001348056.2:c.594G>A
|
NP_001334985.1:p.Leu198=
|
|
NM_001348059.2:c.480G>A
|
NP_001334988.1:p.Leu160=
|
|
NM_001348060.2:c.336G>A
|
NP_001334989.1:p.Leu112=
|
|
NM_003467.3:c.381G>A
MANE Select
|
NP_003458.1:p.Leu127=
|
|