ENST00000696136.1:c.396G>A
|
ENSP00000512428.1:p.Leu132=
|
|
ENST00000696137.1:c.363G>A
|
ENSP00000512429.1:p.Leu121=
|
|
ENST00000696152.1:c.363G>A
|
ENSP00000512443.1:p.Leu121=
|
|
ENST00000696228.1:c.396G>A
|
ENSP00000512494.1:p.Leu132=
|
|
ENST00000241393.4:c.408G>A
MANE Select
|
ENSP00000241393.3:p.Leu136=
|
|
ENST00000241393.3:c.408G>A
|
ENSP00000241393.3:p.Leu136=
|
|
ENST00000409817.1:c.420G>A
|
ENSP00000386884.1:p.Leu140=
|
|
ENST00000466288.1:n.602G>A
|
|
|
NM_001008540.1:c.420G>A
|
NP_001008540.1:p.Leu140=
|
|
NM_003467.2:c.408G>A , LRG_51t1:c.408G>A
|
NP_003458.1:p.Leu136=
|
|
NM_001008540.2:c.420G>A
|
NP_001008540.1:p.Leu140=
|
|
NM_001348056.1:c.621G>A
|
NP_001334985.1:p.Leu207=
|
|
NM_001348059.1:c.507G>A
|
NP_001334988.1:p.Leu169=
|
|
NM_001348060.1:c.363G>A
|
NP_001334989.1:p.Leu121=
|
|
NM_001348056.2:c.621G>A
|
NP_001334985.1:p.Leu207=
|
|
NM_001348059.2:c.507G>A
|
NP_001334988.1:p.Leu169=
|
|
NM_001348060.2:c.363G>A
|
NP_001334989.1:p.Leu121=
|
|
NM_003467.3:c.408G>A
MANE Select
|
NP_003458.1:p.Leu136=
|
|