ENST00000348974.5:c.893A>T
|
ENSP00000330021.7:p.Glu298Val
|
|
ENST00000394236.9:c.893A>T
MANE Select
|
ENSP00000377783.3:p.Glu298Val
|
|
ENST00000407433.6:c.848A>T
|
ENSP00000385794.2:p.Glu283Val
|
|
ENST00000647936.1:c.893A>T
|
ENSP00000496822.1:p.Glu298Val
|
|
ENST00000648381.1:n.1061A>T
|
|
|
ENST00000648853.1:c.851A>T
|
ENSP00000497262.1:p.Glu284Val
|
|
ENST00000649103.1:c.992A>T
|
ENSP00000497962.1:n.992A>T
|
|
ENST00000650591.1:c.989A>T
|
ENSP00000497376.1:p.Glu330Val
|
|
ENST00000394236.7:c.893A>T
|
ENSP00000377783.3:p.Glu298Val
|
|
ENST00000407433.5:c.500A>T
|
ENSP00000385794.1:p.Glu167Val
|
|
NM_000313.3:c.893A>T , LRG_572t1:c.893A>T
|
NP_000304.2:p.Glu298Val
|
|
NM_001314077.1:c.989A>T , LRG_572t2:c.989A>T
|
NP_001301006.1:p.Glu330Val
|
|
NM_000313.4:c.893A>T
MANE Select
|
NP_000304.2:p.Glu298Val
|
|
NM_001314077.2:c.989A>T
|
NP_001301006.1:p.Glu330Val
|
|