ENST00000270301.12:c.2986G>A
|
ENSP00000270301.6:p.Glu996Lys
|
|
ENST00000401500.7:c.2986G>A
MANE Select
|
ENSP00000384792.1:p.Glu996Lys
|
|
ENST00000587391.6:c.*2022G>A
|
ENSP00000465525.1:n.*2022G>A
|
|
ENST00000679357.1:c.776G>A
|
|
|
ENST00000679422.1:c.762-336G>A
|
|
|
ENST00000679682.1:c.2971G>A
|
ENSP00000506226.1:p.Glu991Lys
|
|
ENST00000679714.1:c.2980G>A
|
ENSP00000506627.1:p.Glu994Lys
|
|
ENST00000679757.1:c.2635G>A
|
ENSP00000505158.1:p.Glu879Lys
|
|
ENST00000679858.1:c.*2129G>A
|
ENSP00000505655.1:n.*2129G>A
|
|
ENST00000680211.1:c.-414G>A
|
ENSP00000506102.1:n.-414G>A
|
|
ENST00000680349.1:n.969G>A
|
|
|
ENST00000680403.1:c.2986G>A
|
ENSP00000505677.1:p.Glu996Lys
|
|
ENST00000680564.1:c.2971+361G>A
|
ENSP00000505582.1:n.2971+361G>A
|
|
ENST00000680590.1:c.*1381G>A
|
ENSP00000505350.1:n.*1381G>A
|
|
ENST00000680773.1:n.663G>A
|
|
|
ENST00000680806.1:c.*1801-336G>A
|
ENSP00000506418.1:n.*1801-336G>A
|
|
ENST00000680997.1:n.333G>A
|
|
|
ENST00000681088.1:c.648G>A
|
|
|
ENST00000681625.1:c.*318G>A
|
ENSP00000505555.1:n.*318G>A
|
|
ENST00000270301.11:c.2986G>A
|
ENSP00000270301.6:p.Glu996Lys
|
|
ENST00000401500.6:c.2986G>A
|
ENSP00000384792.1:p.Glu996Lys
|
|
ENST00000587391.5:c.*2022G>A
|
ENSP00000465525.1:n.*2022G>A
|
|
NM_001083961.1:c.2986G>A
|
NP_001077430.1:p.Glu996Lys
|
|
NM_173636.4:c.2986G>A
|
NP_775907.4:p.Glu996Lys
|
|
XM_005258809.2:c.2972-336G>A
|
XP_005258866.1:n.2972-336G>A
|
|
XM_011526837.1:c.2971G>A
|
XP_011525139.1:p.Glu991Lys
|
|
XM_011526838.1:c.2971+361G>A
|
XP_011525140.1:n.2971+361G>A
|
|
XM_011526839.1:c.2635G>A
|
XP_011525141.1:p.Glu879Lys
|
|
XM_011526840.1:c.1978G>A
|
XP_011525142.1:p.Glu660Lys
|
|
XM_011526841.1:c.1564G>A
|
XP_011525143.1:p.Glu522Lys
|
|
XM_011526842.1:c.1417G>A
|
XP_011525144.1:p.Glu473Lys
|
|
XM_011526843.1:c.733G>A
|
XP_011525145.1:p.Glu245Lys
|
|
XM_011526844.1:c.733G>A
|
XP_011525146.1:p.Glu245Lys
|
|
XM_011526840.2:c.1978G>A
|
XP_011525142.1:p.Glu660Lys
|
|
XM_011526841.2:c.1564G>A
|
XP_011525143.1:p.Glu522Lys
|
|
XM_011526844.2:c.733G>A
|
XP_011525146.1:p.Glu245Lys
|
|
XM_017026665.1:c.2986G>A
|
XP_016882154.1:p.Glu996Lys
|
|
NM_001083961.2:c.2986G>A
MANE Select
|
NP_001077430.1:p.Glu996Lys
|
|
NM_173636.5:c.2986G>A
|
NP_775907.4:p.Glu996Lys
|
|