ENST00000206249.8:c.1683G>T
MANE Select
|
ENSP00000206249.3:p.Glu561Asp
|
|
ENST00000641399.1:n.1011G>T
|
|
|
ENST00000206249.7:c.1683G>T
|
ENSP00000206249.3:p.Glu561Asp
|
|
ENST00000338799.9:c.1683G>T
|
ENSP00000342630.5:p.Glu561Asp
|
|
ENST00000406599.5:c.900G>T
|
ENSP00000384064.1:p.Glu300Asp
|
|
ENST00000427531.6:c.851-26405G>T
|
ENSP00000394721.2:n.851-26405G>T
|
|
ENST00000440973.5:c.1683G>T
|
ENSP00000405330.1:p.Glu561Asp
|
|
ENST00000443427.5:c.1683G>T
|
ENSP00000387500.1:p.Glu561Asp
|
|
ENST00000456483.3:c.*558G>T
|
ENSP00000415934.3:n.*558G>T
|
|
NM_000125.3:c.1683G>T
|
NP_000116.2:p.Glu561Asp
|
|
NM_001122740.1:c.1683G>T
|
NP_001116212.1:p.Glu561Asp
|
|
NM_001122741.1:c.1683G>T
|
NP_001116213.1:p.Glu561Asp
|
|
NM_001122742.1:c.1683G>T
|
NP_001116214.1:p.Glu561Asp
|
|
NM_001291230.1:c.1689G>T
|
NP_001278159.1:p.Glu563Asp
|
|
NM_001291241.1:c.1680G>T
|
NP_001278170.1:p.Glu560Asp
|
|
XM_006715374.2:c.*98G>T
|
XP_006715437.1:n.*98G>T
|
|
XM_006715375.2:c.1164G>T
|
XP_006715438.1:p.Glu388Asp
|
|
XM_011535543.1:c.1683G>T
|
XP_011533845.1:p.Glu561Asp
|
|
XM_011535544.1:c.1683G>T
|
XP_011533846.1:p.Glu561Asp
|
|
XM_011535545.1:c.1683G>T
|
XP_011533847.1:p.Glu561Asp
|
|
XM_011535546.1:c.1683G>T
|
XP_011533848.1:p.Glu561Asp
|
|
XM_011535548.1:c.1164G>T
|
XP_011533850.1:p.Glu388Asp
|
|
XM_011535549.1:c.954G>T
|
XP_011533851.1:p.Glu318Asp
|
|
NM_001328100.1:c.851-26405G>T
|
NP_001315029.1:n.851-26405G>T
|
|
XM_006715374.3:c.*98G>T
|
XP_006715437.1:n.*98G>T
|
|
XM_006715375.3:c.1164G>T
|
XP_006715438.1:p.Glu388Asp
|
|
XM_011535543.2:c.1683G>T
|
XP_011533845.1:p.Glu561Asp
|
|
XM_011535544.2:c.1683G>T
|
XP_011533846.1:p.Glu561Asp
|
|
XM_011535545.2:c.1683G>T
|
XP_011533847.1:p.Glu561Asp
|
|
XM_011535549.2:c.954G>T
|
XP_011533851.1:p.Glu318Asp
|
|
XM_017010376.1:c.1683G>T
|
XP_016865865.1:p.Glu561Asp
|
|
XM_017010377.1:c.1683G>T
|
XP_016865866.1:p.Glu561Asp
|
|
XM_017010378.1:c.1683G>T
|
XP_016865867.1:p.Glu561Asp
|
|
XM_017010379.1:c.1683G>T
|
XP_016865868.1:p.Glu561Asp
|
|
XM_017010380.1:c.1683G>T
|
XP_016865869.1:p.Glu561Asp
|
|
XM_017010381.1:c.1683G>T
|
XP_016865870.1:p.Glu561Asp
|
|
XM_017010382.2:c.1026G>T
|
XP_016865871.1:p.Glu342Asp
|
|
XM_017010383.1:c.894G>T
|
XP_016865872.1:p.Glu298Asp
|
|
XR_001743223.2:n.1730G>T
|
|
|
NM_000125.4:c.1683G>T
MANE Select
|
NP_000116.2:p.Glu561Asp
|
|
NM_001328100.2:c.851-26405G>T
|
NP_001315029.1:n.851-26405G>T
|
|
NM_001122740.2:c.1683G>T
|
NP_001116212.1:p.Glu561Asp
|
|
NM_001122741.2:c.1683G>T
|
NP_001116213.1:p.Glu561Asp
|
|
NM_001122742.2:c.1683G>T
|
NP_001116214.1:p.Glu561Asp
|
|
NM_001291230.2:c.1689G>T
|
NP_001278159.1:p.Glu563Asp
|
|
NM_001291241.2:c.1680G>T
|
NP_001278170.1:p.Glu560Asp
|
|
NM_001385568.1:c.1683G>T
|
NP_001372497.1:p.Glu561Asp
|
|
NM_001385569.1:c.1683G>T
|
NP_001372498.1:p.Glu561Asp
|
|
NM_001385570.1:c.*98G>T
|
NP_001372499.1:n.*98G>T
|
|
NM_001385571.1:c.*98G>T
|
NP_001372500.1:n.*98G>T
|
|
NM_001385572.1:c.*98G>T
|
NP_001372501.1:n.*98G>T
|
|