ENST00000270301.12:c.4173C>A
|
ENSP00000270301.6:p.Arg1391=
|
|
ENST00000401500.7:c.4188C>A
MANE Select
|
ENSP00000384792.1:p.Arg1396=
|
|
ENST00000587391.6:c.*4048C>A
|
ENSP00000465525.1:n.*4048C>A
|
|
ENST00000679357.1:c.2268C>A
|
|
|
ENST00000679598.1:c.933C>A
|
|
|
ENST00000679682.1:c.4173C>A
|
ENSP00000506226.1:p.Arg1391=
|
|
ENST00000679714.1:c.4182C>A
|
ENSP00000506627.1:p.Arg1394=
|
|
ENST00000679757.1:c.3837C>A
|
ENSP00000505158.1:p.Arg1279=
|
|
ENST00000679858.1:c.*3570C>A
|
ENSP00000505655.1:n.*3570C>A
|
|
ENST00000680211.1:c.789C>A
|
ENSP00000506102.1:p.Arg263=
|
|
ENST00000680280.1:n.1691C>A
|
|
|
ENST00000680349.1:n.2837C>A
|
|
|
ENST00000680403.1:c.4173C>A
|
ENSP00000505677.1:p.Arg1391=
|
|
ENST00000680564.1:c.3939C>A
|
ENSP00000505582.1:p.Arg1313=
|
|
ENST00000680590.1:c.*2568C>A
|
ENSP00000505350.1:n.*2568C>A
|
|
ENST00000680597.1:c.921C>A
|
|
|
ENST00000680739.1:c.1203C>A
|
|
|
ENST00000680773.1:n.2689C>A
|
|
|
ENST00000680806.1:c.*3491C>A
|
ENSP00000506418.1:n.*3491C>A
|
|
ENST00000680997.1:n.2120C>A
|
|
|
ENST00000681608.1:n.2033C>A
|
|
|
ENST00000681625.1:c.*1520C>A
|
ENSP00000505555.1:n.*1520C>A
|
|
ENST00000681648.1:n.2239C>A
|
|
|
ENST00000270301.11:c.4173C>A
|
ENSP00000270301.6:p.Arg1391=
|
|
ENST00000401500.6:c.4188C>A
|
ENSP00000384792.1:p.Arg1396=
|
|
ENST00000587391.5:c.*4048C>A
|
ENSP00000465525.1:n.*4048C>A
|
|
NM_001083961.1:c.4188C>A
|
NP_001077430.1:p.Arg1396=
|
|
NM_173636.4:c.4173C>A
|
NP_775907.4:p.Arg1391=
|
|
XM_005258809.2:c.4077C>A
|
XP_005258866.1:p.Arg1359=
|
|
XM_011526837.1:c.4173C>A
|
XP_011525139.1:p.Arg1391=
|
|
XM_011526838.1:c.3939C>A
|
XP_011525140.1:p.Arg1313=
|
|
XM_011526839.1:c.3837C>A
|
XP_011525141.1:p.Arg1279=
|
|
XM_011526840.1:c.3180C>A
|
XP_011525142.1:p.Arg1060=
|
|
XM_011526841.1:c.2766C>A
|
XP_011525143.1:p.Arg922=
|
|
XM_011526842.1:c.2619C>A
|
XP_011525144.1:p.Arg873=
|
|
XM_011526843.1:c.1935C>A
|
XP_011525145.1:p.Arg645=
|
|
XM_011526844.1:c.1935C>A
|
XP_011525146.1:p.Arg645=
|
|
XM_011526840.2:c.3180C>A
|
XP_011525142.1:p.Arg1060=
|
|
XM_011526841.2:c.2766C>A
|
XP_011525143.1:p.Arg922=
|
|
XM_011526844.2:c.1935C>A
|
XP_011525146.1:p.Arg645=
|
|
XM_017026665.1:c.4188C>A
|
XP_016882154.1:p.Arg1396=
|
|
NM_001083961.2:c.4188C>A
MANE Select
|
NP_001077430.1:p.Arg1396=
|
|
NM_173636.5:c.4173C>A
|
NP_775907.4:p.Arg1391=
|
|