ENST00000270301.12:c.3090A>T
|
ENSP00000270301.6:p.Ala1030=
|
|
ENST00000401500.7:c.3090A>T
MANE Select
|
ENSP00000384792.1:p.Ala1030=
|
|
ENST00000587391.6:c.*2365A>T
|
ENSP00000465525.1:n.*2365A>T
|
|
ENST00000679357.1:c.880A>T
|
|
|
ENST00000679422.1:c.769A>T
|
|
|
ENST00000679682.1:c.3075A>T
|
ENSP00000506226.1:p.Ala1025=
|
|
ENST00000679714.1:c.3084A>T
|
ENSP00000506627.1:p.Ala1028=
|
|
ENST00000679757.1:c.2739A>T
|
ENSP00000505158.1:p.Ala913=
|
|
ENST00000679858.1:c.*2472A>T
|
ENSP00000505655.1:n.*2472A>T
|
|
ENST00000680211.1:c.-310A>T
|
ENSP00000506102.1:n.-310A>T
|
|
ENST00000680349.1:n.1073A>T
|
|
|
ENST00000680403.1:c.3090A>T
|
ENSP00000505677.1:p.Ala1030=
|
|
ENST00000680564.1:c.2971+704A>T
|
ENSP00000505582.1:n.2971+704A>T
|
|
ENST00000680590.1:c.*1485A>T
|
ENSP00000505350.1:n.*1485A>T
|
|
ENST00000680739.1:c.8A>T
|
|
|
ENST00000680773.1:n.1006A>T
|
|
|
ENST00000680806.1:c.*1808A>T
|
ENSP00000506418.1:n.*1808A>T
|
|
ENST00000680997.1:n.437A>T
|
|
|
ENST00000681088.1:c.752A>T
|
|
|
ENST00000681608.1:n.38A>T
|
|
|
ENST00000681625.1:c.*422A>T
|
ENSP00000505555.1:n.*422A>T
|
|
ENST00000270301.11:c.3090A>T
|
ENSP00000270301.6:p.Ala1030=
|
|
ENST00000401500.6:c.3090A>T
|
ENSP00000384792.1:p.Ala1030=
|
|
ENST00000587391.5:c.*2365A>T
|
ENSP00000465525.1:n.*2365A>T
|
|
NM_001083961.1:c.3090A>T
|
NP_001077430.1:p.Ala1030=
|
|
NM_173636.4:c.3090A>T
|
NP_775907.4:p.Ala1030=
|
|
XM_005258809.2:c.2979A>T
|
XP_005258866.1:p.Ala993=
|
|
XM_011526837.1:c.3075A>T
|
XP_011525139.1:p.Ala1025=
|
|
XM_011526838.1:c.2971+704A>T
|
XP_011525140.1:n.2971+704A>T
|
|
XM_011526839.1:c.2739A>T
|
XP_011525141.1:p.Ala913=
|
|
XM_011526840.1:c.2082A>T
|
XP_011525142.1:p.Ala694=
|
|
XM_011526841.1:c.1668A>T
|
XP_011525143.1:p.Ala556=
|
|
XM_011526842.1:c.1521A>T
|
XP_011525144.1:p.Ala507=
|
|
XM_011526843.1:c.837A>T
|
XP_011525145.1:p.Ala279=
|
|
XM_011526844.1:c.837A>T
|
XP_011525146.1:p.Ala279=
|
|
XM_011526840.2:c.2082A>T
|
XP_011525142.1:p.Ala694=
|
|
XM_011526841.2:c.1668A>T
|
XP_011525143.1:p.Ala556=
|
|
XM_011526844.2:c.837A>T
|
XP_011525146.1:p.Ala279=
|
|
XM_017026665.1:c.3090A>T
|
XP_016882154.1:p.Ala1030=
|
|
NM_001083961.2:c.3090A>T
MANE Select
|
NP_001077430.1:p.Ala1030=
|
|
NM_173636.5:c.3090A>T
|
NP_775907.4:p.Ala1030=
|
|