ENST00000380707.9:c.856G>A
MANE Select
|
ENSP00000370083.4:p.Glu286Lys
|
|
ENST00000351205.8:c.856G>A
|
ENSP00000305857.5:p.Glu286Lys
|
|
ENST00000380707.8:c.856G>A
|
ENSP00000370083.4:p.Glu286Lys
|
|
ENST00000503079.6:c.760G>A
|
ENSP00000428128.1:p.Glu254Lys
|
|
ENST00000506163.5:c.835-477G>A
|
ENSP00000424926.1:n.835-477G>A
|
|
ENST00000506239.6:c.*59-477G>A
|
ENSP00000422679.2:n.*59-477G>A
|
|
ENST00000510679.1:n.110G>A
|
|
|
ENST00000514951.5:c.655G>A
|
ENSP00000423298.1:p.Glu219Lys
|
|
NM_000344.3:c.856G>A , LRG_676t1:c.856G>A
|
NP_000335.1:p.Glu286Lys
|
|
NM_001297715.1:c.835-477G>A
|
NP_001284644.1:n.835-477G>A
|
|
NM_022874.2:c.760G>A
|
NP_075012.1:p.Glu254Lys
|
|
XM_011543597.1:c.655G>A
|
XP_011541899.1:p.Glu219Lys
|
|
XM_011543598.1:c.559G>A
|
XP_011541900.1:p.Glu187Lys
|
|
XM_011543598.3:c.559G>A
|
XP_011541900.1:p.Glu187Lys
|
|
XM_017009786.1:c.739-477G>A
|
XP_016865275.1:n.739-477G>A
|
|
NM_000344.4:c.856G>A
MANE Select
|
NP_000335.1:p.Glu286Lys
|
|