ENST00000519811.6:c.1886C>T
MANE Select
|
ENSP00000428714.1:p.Ala629Val
|
|
ENST00000262585.6:c.1646C>T
|
ENSP00000262585.2:p.Ala549Val
|
|
ENST00000424248.2:c.1490C>T
|
ENSP00000410594.1:p.Ala497Val
|
|
ENST00000518668.5:c.1659C>T
|
|
|
ENST00000519811.5:c.1886C>T
|
ENSP00000428714.1:p.Ala629Val
|
|
ENST00000520482.1:n.1427C>T
|
|
|
NM_014957.2:c.1646C>T
|
NP_055772.2:p.Ala549Val
|
|
XM_005250838.3:c.1685C>T
|
XP_005250895.2:p.Ala562Val
|
|
XM_005250839.2:c.1685C>T
|
XP_005250896.2:p.Ala562Val
|
|
XM_005250840.3:c.1529C>T
|
XP_005250897.2:p.Ala510Val
|
|
XM_005250841.2:c.1529C>T
|
XP_005250898.2:p.Ala510Val
|
|
XM_005250842.3:c.1652C>T
|
XP_005250899.1:p.Ala551Val
|
|
XM_005250843.3:c.1142C>T
|
XP_005250900.1:p.Ala381Val
|
|
XM_011516933.1:c.1685C>T
|
XP_011515235.1:p.Ala562Val
|
|
XM_011516934.1:c.1685C>T
|
XP_011515236.1:p.Ala562Val
|
|
XM_011516935.1:c.1319C>T
|
XP_011515237.1:p.Ala440Val
|
|
XM_011516936.1:c.1313C>T
|
XP_011515238.1:p.Ala438Val
|
|
XM_011516937.1:c.1685C>T
|
XP_011515239.1:p.Ala562Val
|
|
XM_011516938.1:c.854C>T
|
XP_011515240.1:p.Ala285Val
|
|
XM_011516939.1:c.383C>T
|
XP_011515241.1:p.Ala128Val
|
|
XM_011516940.1:c.383C>T
|
XP_011515242.1:p.Ala128Val
|
|
XM_011516941.1:c.1685C>T
|
XP_011515243.1:p.Ala562Val
|
|
XM_011516942.1:c.1685C>T
|
XP_011515244.1:p.Ala562Val
|
|
XR_242384.2:n.1815C>T
|
|
|
XR_928310.1:n.1815C>T
|
|
|
XR_928311.1:n.1815C>T
|
|
|
XR_928312.1:n.1815C>T
|
|
|
NM_001352890.2:c.1886C>T
|
NP_001339819.2:p.Ala629Val
|
|
NM_001362798.1:c.1886C>T
|
NP_001349727.1:p.Ala629Val
|
|
NM_014957.4:c.1685C>T
|
NP_055772.3:p.Ala562Val
|
|
NR_148197.2:n.1982C>T
|
|
|
XM_005250840.5:c.1730C>T
|
XP_005250897.3:p.Ala577Val
|
|
XM_005250841.4:c.1730C>T
|
XP_005250898.3:p.Ala577Val
|
|
XM_005250842.4:c.1652C>T
|
XP_005250899.1:p.Ala551Val
|
|
XM_011516933.2:c.1886C>T
|
XP_011515235.2:p.Ala629Val
|
|
XM_011516934.3:c.1886C>T
|
XP_011515236.2:p.Ala629Val
|
|
XM_011516937.2:c.1886C>T
|
XP_011515239.2:p.Ala629Val
|
|
XM_011516938.3:c.854C>T
|
XP_011515240.1:p.Ala285Val
|
|
XM_011516939.3:c.383C>T
|
XP_011515241.1:p.Ala128Val
|
|
XM_011516940.2:c.383C>T
|
XP_011515242.1:p.Ala128Val
|
|
XM_011516941.3:c.1886C>T
|
XP_011515243.2:p.Ala629Val
|
|
XM_017013241.1:c.1685C>T
|
XP_016868730.1:p.Ala562Val
|
|
XM_017013242.1:c.1142C>T
|
XP_016868731.1:p.Ala381Val
|
|
XM_017013243.1:c.422C>T
|
XP_016868732.1:p.Ala141Val
|
|
XR_001745497.2:n.2032C>T
|
|
|
XR_001745498.2:n.2032C>T
|
|
|
XR_928310.3:n.2032C>T
|
|
|
XR_928312.3:n.2032C>T
|
|
|
NM_001352890.3:c.1886C>T
MANE Select
|
NP_001339819.2:p.Ala629Val
|
|
NM_001362798.2:c.1886C>T
|
NP_001349727.1:p.Ala629Val
|
|
NM_014957.5:c.1685C>T
|
NP_055772.3:p.Ala562Val
|
|
NR_148197.3:n.2005C>T
|
|
|