ENST00000270301.12:c.3311A=
|
ENSP00000270301.6:p.Lys1104=
|
|
ENST00000401500.7:c.3326A=
MANE Select
|
ENSP00000384792.1:p.Lys1109=
|
|
ENST00000587391.6:c.*3186A=
|
ENSP00000465525.1:n.*3186A=
|
|
ENST00000679357.1:c.1406A=
|
|
|
ENST00000679598.1:c.91A=
|
|
|
ENST00000679682.1:c.3311A=
|
ENSP00000506226.1:p.Lys1104=
|
|
ENST00000679714.1:c.3320A=
|
ENSP00000506627.1:p.Lys1107=
|
|
ENST00000679757.1:c.2975A=
|
ENSP00000505158.1:p.Lys992=
|
|
ENST00000679858.1:c.*2708A=
|
ENSP00000505655.1:n.*2708A=
|
|
ENST00000680211.1:c.-74A=
|
ENSP00000506102.1:n.-74A=
|
|
ENST00000680280.1:n.613A=
|
|
|
ENST00000680349.1:n.1894A=
|
|
|
ENST00000680403.1:c.3311A=
|
ENSP00000505677.1:p.Lys1104=
|
|
ENST00000680564.1:c.3077A=
|
ENSP00000505582.1:p.Lys1026=
|
|
ENST00000680590.1:c.*1706A=
|
ENSP00000505350.1:n.*1706A=
|
|
ENST00000680597.1:c.91A=
|
|
|
ENST00000680739.1:c.341A=
|
|
|
ENST00000680773.1:n.1827A=
|
|
|
ENST00000680806.1:c.*2629A=
|
ENSP00000506418.1:n.*2629A=
|
|
ENST00000680997.1:n.1258A=
|
|
|
ENST00000681608.1:n.859A=
|
|
|
ENST00000681625.1:c.*658A=
|
ENSP00000505555.1:n.*658A=
|
|
ENST00000681648.1:n.625A=
|
|
|
ENST00000270301.11:c.3311A=
|
ENSP00000270301.6:p.Lys1104=
|
|
ENST00000401500.6:c.3326A=
|
ENSP00000384792.1:p.Lys1109=
|
|
ENST00000587391.5:c.*3186A=
|
ENSP00000465525.1:n.*3186A=
|
|
NM_001083961.1:c.3326A=
|
NP_001077430.1:p.Lys1109=
|
|
NM_173636.4:c.3311A=
|
NP_775907.4:p.Lys1104=
|
|
XM_005258809.2:c.3215A=
|
XP_005258866.1:p.Lys1072=
|
|
XM_011526837.1:c.3311A=
|
XP_011525139.1:p.Lys1104=
|
|
XM_011526838.1:c.3077A=
|
XP_011525140.1:p.Lys1026=
|
|
XM_011526839.1:c.2975A=
|
XP_011525141.1:p.Lys992=
|
|
XM_011526840.1:c.2318A=
|
XP_011525142.1:p.Lys773=
|
|
XM_011526841.1:c.1904A=
|
XP_011525143.1:p.Lys635=
|
|
XM_011526842.1:c.1757A=
|
XP_011525144.1:p.Lys586=
|
|
XM_011526843.1:c.1073A=
|
XP_011525145.1:p.Lys358=
|
|
XM_011526844.1:c.1073A=
|
XP_011525146.1:p.Lys358=
|
|
XM_011526840.2:c.2318A=
|
XP_011525142.1:p.Lys773=
|
|
XM_011526841.2:c.1904A=
|
XP_011525143.1:p.Lys635=
|
|
XM_011526844.2:c.1073A=
|
XP_011525146.1:p.Lys358=
|
|
XM_017026665.1:c.3326A=
|
XP_016882154.1:p.Lys1109=
|
|
NM_001083961.2:c.3326A=
MANE Select
|
NP_001077430.1:p.Lys1109=
|
|
NM_173636.5:c.3311A=
|
NP_775907.4:p.Lys1104=
|
|