|
ENST00000260947.9:c.2293G>T
MANE Select
|
ENSP00000260947.4:p.Asp765Tyr
|
|
|
ENST00000421162.2:c.940G>T
|
ENSP00000392245.2:p.Asp314Tyr
|
|
|
ENST00000613192.2:c.*356G>T
|
ENSP00000483275.2:n.*356G>T
|
|
|
ENST00000613374.5:c.883G>T
|
ENSP00000484464.1:p.Asp295Tyr
|
|
|
ENST00000613706.5:c.1885G>T
|
ENSP00000484976.2:p.Asp629Tyr
|
|
|
ENST00000617164.5:c.2236G>T
|
ENSP00000480470.1:p.Asp746Tyr
|
|
|
ENST00000619009.5:c.754G>T
|
ENSP00000482293.1:p.Asp252Tyr
|
|
|
ENST00000650978.1:c.3668G>T
|
|
|
|
ENST00000260947.8:c.2293G>T
|
ENSP00000260947.4:p.Asp765Tyr
|
|
|
ENST00000432456.5:c.436G>T
|
|
|
|
ENST00000455743.5:c.*1913G>T
|
ENSP00000412186.1:n.*1913G>T
|
|
|
ENST00000471590.5:n.628G>T
|
|
|
|
ENST00000613192.1:c.463G>T
|
ENSP00000483275.1:p.Asp155Tyr
|
|
|
ENST00000613374.4:c.883G>T
|
ENSP00000484464.1:p.Asp295Tyr
|
|
|
ENST00000613706.4:c.940G>T
|
ENSP00000484976.1:p.Asp314Tyr
|
|
|
ENST00000617164.4:c.2236G>T
|
ENSP00000480470.1:p.Asp746Tyr
|
|
|
ENST00000619009.4:c.754G>T
|
ENSP00000482293.1:p.Asp252Tyr
|
|
|
ENST00000620057.4:c.*959G>T
|
ENSP00000481988.1:n.*959G>T
|
|
|
NM_000465.3:c.2293G>T
|
NP_000456.2:p.Asp765Tyr
|
|
|
NM_001282543.1:c.2236G>T
|
NP_001269472.1:p.Asp746Tyr
|
|
|
NM_001282545.1:c.940G>T
|
NP_001269474.1:p.Asp314Tyr
|
|
|
NM_001282548.1:c.883G>T
|
NP_001269477.1:p.Asp295Tyr
|
|
|
NM_001282549.1:c.754G>T
|
NP_001269478.1:p.Asp252Tyr
|
|
|
NR_104212.1:n.2286G>T
|
|
|
|
NR_104215.1:n.2229G>T
|
|
|
|
NR_104216.1:n.1485G>T
|
|
|
|
XM_011511567.1:c.2239G>T
|
XP_011509869.1:p.Asp747Tyr
|
|
|
XM_017004613.1:c.2392G>T
|
XP_016860102.1:p.Asp798Tyr
|
|
|
XR_002959322.1:n.2659G>T
|
|
|
|
NM_000465.4:c.2293G>T
MANE Select
|
NP_000456.2:p.Asp765Tyr
|
|
|
NM_001282543.2:c.2236G>T
|
NP_001269472.1:p.Asp746Tyr
|
|
|
NM_001282545.2:c.940G>T
|
NP_001269474.1:p.Asp314Tyr
|
|
|
NM_001282548.2:c.883G>T
|
NP_001269477.1:p.Asp295Tyr
|
|
|
NM_001282549.2:c.754G>T
|
NP_001269478.1:p.Asp252Tyr
|
|
|
NR_104212.2:n.2258G>T
|
|
|
|
NR_104215.2:n.2201G>T
|
|
|
|
NR_104216.2:n.1457G>T
|
|
|
