ENST00000696136.1:c.386A>T
|
ENSP00000512428.1:p.Asp129Val
|
|
ENST00000696137.1:c.353A>T
|
ENSP00000512429.1:p.Asp118Val
|
|
ENST00000696152.1:c.353A>T
|
ENSP00000512443.1:p.Asp118Val
|
|
ENST00000696228.1:c.386A>T
|
ENSP00000512494.1:p.Asp129Val
|
|
ENST00000241393.4:c.398A>T
MANE Select
|
ENSP00000241393.3:p.Asp133Val
|
|
ENST00000241393.3:c.398A>T
|
ENSP00000241393.3:p.Asp133Val
|
|
ENST00000409817.1:c.410A>T
|
ENSP00000386884.1:p.Asp137Val
|
|
ENST00000466288.1:n.592A>T
|
|
|
NM_001008540.1:c.410A>T
|
NP_001008540.1:p.Asp137Val
|
|
NM_003467.2:c.398A>T , LRG_51t1:c.398A>T
|
NP_003458.1:p.Asp133Val
|
|
NM_001008540.2:c.410A>T
|
NP_001008540.1:p.Asp137Val
|
|
NM_001348056.1:c.611A>T
|
NP_001334985.1:p.Asp204Val
|
|
NM_001348059.1:c.497A>T
|
NP_001334988.1:p.Asp166Val
|
|
NM_001348060.1:c.353A>T
|
NP_001334989.1:p.Asp118Val
|
|
NM_001348056.2:c.611A>T
|
NP_001334985.1:p.Asp204Val
|
|
NM_001348059.2:c.497A>T
|
NP_001334988.1:p.Asp166Val
|
|
NM_001348060.2:c.353A>T
|
NP_001334989.1:p.Asp118Val
|
|
NM_003467.3:c.398A>T
MANE Select
|
NP_003458.1:p.Asp133Val
|
|