ENST00000348974.5:c.1922A>T
|
ENSP00000330021.7:p.Glu641Val
|
|
ENST00000394236.9:c.1922A>T
MANE Select
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ENSP00000377783.3:p.Glu641Val
|
|
ENST00000407433.6:c.1877A>T
|
ENSP00000385794.2:p.Glu626Val
|
|
ENST00000647936.1:c.*25A>T
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ENSP00000496822.1:n.*25A>T
|
|
ENST00000648381.1:n.2090A>T
|
|
|
ENST00000648853.1:c.1880A>T
|
ENSP00000497262.1:p.Glu627Val
|
|
ENST00000650591.1:c.2018A>T
|
ENSP00000497376.1:p.Glu673Val
|
|
ENST00000394236.7:c.1922A>T
|
ENSP00000377783.3:p.Glu641Val
|
|
ENST00000407433.5:c.1529A>T
|
ENSP00000385794.1:p.Glu510Val
|
|
NM_000313.3:c.1922A>T , LRG_572t1:c.1922A>T
|
NP_000304.2:p.Glu641Val
|
|
NM_001314077.1:c.2018A>T , LRG_572t2:c.2018A>T
|
NP_001301006.1:p.Glu673Val
|
|
NM_000313.4:c.1922A>T
MANE Select
|
NP_000304.2:p.Glu641Val
|
|
NM_001314077.2:c.2018A>T
|
NP_001301006.1:p.Glu673Val
|
|