ENST00000519811.6:c.2234A>T
MANE Select
|
ENSP00000428714.1:p.Asp745Val
|
|
ENST00000262585.6:c.1994A>T
|
ENSP00000262585.2:p.Asp665Val
|
|
ENST00000424248.2:c.1838A>T
|
ENSP00000410594.1:p.Asp613Val
|
|
ENST00000518668.5:c.2007A>T
|
|
|
ENST00000519811.5:c.2234A>T
|
ENSP00000428714.1:p.Asp745Val
|
|
ENST00000520482.1:n.1775A>T
|
|
|
NM_014957.2:c.1994A>T
|
NP_055772.2:p.Asp665Val
|
|
XM_005250838.3:c.2033A>T
|
XP_005250895.2:p.Asp678Val
|
|
XM_005250839.2:c.2033A>T
|
XP_005250896.2:p.Asp678Val
|
|
XM_005250840.3:c.1877A>T
|
XP_005250897.2:p.Asp626Val
|
|
XM_005250841.2:c.1877A>T
|
XP_005250898.2:p.Asp626Val
|
|
XM_005250842.3:c.2000A>T
|
XP_005250899.1:p.Asp667Val
|
|
XM_005250843.3:c.1490A>T
|
XP_005250900.1:p.Asp497Val
|
|
XM_011516933.1:c.2033A>T
|
XP_011515235.1:p.Asp678Val
|
|
XM_011516934.1:c.2033A>T
|
XP_011515236.1:p.Asp678Val
|
|
XM_011516935.1:c.1667A>T
|
XP_011515237.1:p.Asp556Val
|
|
XM_011516936.1:c.1661A>T
|
XP_011515238.1:p.Asp554Val
|
|
XM_011516937.1:c.2033A>T
|
XP_011515239.1:p.Asp678Val
|
|
XM_011516938.1:c.1202A>T
|
XP_011515240.1:p.Asp401Val
|
|
XM_011516939.1:c.731A>T
|
XP_011515241.1:p.Asp244Val
|
|
XM_011516940.1:c.731A>T
|
XP_011515242.1:p.Asp244Val
|
|
XM_011516941.1:c.2033A>T
|
XP_011515243.1:p.Asp678Val
|
|
XM_011516942.1:c.2033A>T
|
XP_011515244.1:p.Asp678Val
|
|
XR_242384.2:n.2163A>T
|
|
|
XR_928310.1:n.2163A>T
|
|
|
XR_928311.1:n.2163A>T
|
|
|
XR_928312.1:n.2163A>T
|
|
|
NM_001352890.2:c.2234A>T
|
NP_001339819.2:p.Asp745Val
|
|
NM_001362798.1:c.2234A>T
|
NP_001349727.1:p.Asp745Val
|
|
NM_014957.4:c.2033A>T
|
NP_055772.3:p.Asp678Val
|
|
NR_148197.2:n.2330A>T
|
|
|
XM_005250840.5:c.2078A>T
|
XP_005250897.3:p.Asp693Val
|
|
XM_005250841.4:c.2078A>T
|
XP_005250898.3:p.Asp693Val
|
|
XM_005250842.4:c.2000A>T
|
XP_005250899.1:p.Asp667Val
|
|
XM_011516933.2:c.2234A>T
|
XP_011515235.2:p.Asp745Val
|
|
XM_011516934.3:c.2234A>T
|
XP_011515236.2:p.Asp745Val
|
|
XM_011516937.2:c.2234A>T
|
XP_011515239.2:p.Asp745Val
|
|
XM_011516938.3:c.1202A>T
|
XP_011515240.1:p.Asp401Val
|
|
XM_011516939.3:c.731A>T
|
XP_011515241.1:p.Asp244Val
|
|
XM_011516940.2:c.731A>T
|
XP_011515242.1:p.Asp244Val
|
|
XM_011516941.3:c.2234A>T
|
XP_011515243.2:p.Asp745Val
|
|
XM_017013241.1:c.2033A>T
|
XP_016868730.1:p.Asp678Val
|
|
XM_017013242.1:c.1490A>T
|
XP_016868731.1:p.Asp497Val
|
|
XM_017013243.1:c.770A>T
|
XP_016868732.1:p.Asp257Val
|
|
XR_001745497.2:n.2380A>T
|
|
|
XR_001745498.2:n.2380A>T
|
|
|
XR_928310.3:n.2380A>T
|
|
|
XR_928312.3:n.2380A>T
|
|
|
NM_001352890.3:c.2234A>T
MANE Select
|
NP_001339819.2:p.Asp745Val
|
|
NM_001362798.2:c.2234A>T
|
NP_001349727.1:p.Asp745Val
|
|
NM_014957.5:c.2033A>T
|
NP_055772.3:p.Asp678Val
|
|
NR_148197.3:n.2353A>T
|
|
|