ENST00000696136.1:c.400A>G
|
ENSP00000512428.1:p.Ile134Val
|
|
ENST00000696137.1:c.367A>G
|
ENSP00000512429.1:p.Ile123Val
|
|
ENST00000696152.1:c.367A>G
|
ENSP00000512443.1:p.Ile123Val
|
|
ENST00000696228.1:c.400A>G
|
ENSP00000512494.1:p.Ile134Val
|
|
ENST00000241393.4:c.412A>G
MANE Select
|
ENSP00000241393.3:p.Ile138Val
|
|
ENST00000241393.3:c.412A>G
|
ENSP00000241393.3:p.Ile138Val
|
|
ENST00000409817.1:c.424A>G
|
ENSP00000386884.1:p.Ile142Val
|
|
ENST00000466288.1:n.606A>G
|
|
|
NM_001008540.1:c.424A>G
|
NP_001008540.1:p.Ile142Val
|
|
NM_003467.2:c.412A>G , LRG_51t1:c.412A>G
|
NP_003458.1:p.Ile138Val
|
|
NM_001008540.2:c.424A>G
|
NP_001008540.1:p.Ile142Val
|
|
NM_001348056.1:c.625A>G
|
NP_001334985.1:p.Ile209Val
|
|
NM_001348059.1:c.511A>G
|
NP_001334988.1:p.Ile171Val
|
|
NM_001348060.1:c.367A>G
|
NP_001334989.1:p.Ile123Val
|
|
NM_001348056.2:c.625A>G
|
NP_001334985.1:p.Ile209Val
|
|
NM_001348059.2:c.511A>G
|
NP_001334988.1:p.Ile171Val
|
|
NM_001348060.2:c.367A>G
|
NP_001334989.1:p.Ile123Val
|
|
NM_003467.3:c.412A>G
MANE Select
|
NP_003458.1:p.Ile138Val
|
|