ENST00000270301.12:c.3210C>G
|
ENSP00000270301.6:p.Ser1070=
|
|
ENST00000401500.7:c.3210C>G
MANE Select
|
ENSP00000384792.1:p.Ser1070=
|
|
ENST00000587391.6:c.*2485C>G
|
ENSP00000465525.1:n.*2485C>G
|
|
ENST00000679357.1:c.1000C>G
|
|
|
ENST00000679422.1:c.889C>G
|
|
|
ENST00000679682.1:c.3195C>G
|
ENSP00000506226.1:p.Ser1065=
|
|
ENST00000679714.1:c.3204C>G
|
ENSP00000506627.1:p.Ser1068=
|
|
ENST00000679757.1:c.2859C>G
|
ENSP00000505158.1:p.Ser953=
|
|
ENST00000679858.1:c.*2592C>G
|
ENSP00000505655.1:n.*2592C>G
|
|
ENST00000680211.1:c.-190C>G
|
ENSP00000506102.1:n.-190C>G
|
|
ENST00000680349.1:n.1193C>G
|
|
|
ENST00000680403.1:c.3210C>G
|
ENSP00000505677.1:p.Ser1070=
|
|
ENST00000680564.1:c.2972-596C>G
|
ENSP00000505582.1:n.2972-596C>G
|
|
ENST00000680590.1:c.*1605C>G
|
ENSP00000505350.1:n.*1605C>G
|
|
ENST00000680739.1:c.128C>G
|
|
|
ENST00000680773.1:n.1126C>G
|
|
|
ENST00000680806.1:c.*1928C>G
|
ENSP00000506418.1:n.*1928C>G
|
|
ENST00000680997.1:n.557C>G
|
|
|
ENST00000681088.1:c.872C>G
|
|
|
ENST00000681608.1:n.158C>G
|
|
|
ENST00000681625.1:c.*542C>G
|
ENSP00000505555.1:n.*542C>G
|
|
ENST00000270301.11:c.3210C>G
|
ENSP00000270301.6:p.Ser1070=
|
|
ENST00000401500.6:c.3210C>G
|
ENSP00000384792.1:p.Ser1070=
|
|
ENST00000587391.5:c.*2485C>G
|
ENSP00000465525.1:n.*2485C>G
|
|
NM_001083961.1:c.3210C>G
|
NP_001077430.1:p.Ser1070=
|
|
NM_173636.4:c.3210C>G
|
NP_775907.4:p.Ser1070=
|
|
XM_005258809.2:c.3099C>G
|
XP_005258866.1:p.Ser1033=
|
|
XM_011526837.1:c.3195C>G
|
XP_011525139.1:p.Ser1065=
|
|
XM_011526838.1:c.2972-596C>G
|
XP_011525140.1:n.2972-596C>G
|
|
XM_011526839.1:c.2859C>G
|
XP_011525141.1:p.Ser953=
|
|
XM_011526840.1:c.2202C>G
|
XP_011525142.1:p.Ser734=
|
|
XM_011526841.1:c.1788C>G
|
XP_011525143.1:p.Ser596=
|
|
XM_011526842.1:c.1641C>G
|
XP_011525144.1:p.Ser547=
|
|
XM_011526843.1:c.957C>G
|
XP_011525145.1:p.Ser319=
|
|
XM_011526844.1:c.957C>G
|
XP_011525146.1:p.Ser319=
|
|
XM_011526840.2:c.2202C>G
|
XP_011525142.1:p.Ser734=
|
|
XM_011526841.2:c.1788C>G
|
XP_011525143.1:p.Ser596=
|
|
XM_011526844.2:c.957C>G
|
XP_011525146.1:p.Ser319=
|
|
XM_017026665.1:c.3210C>G
|
XP_016882154.1:p.Ser1070=
|
|
NM_001083961.2:c.3210C>G
MANE Select
|
NP_001077430.1:p.Ser1070=
|
|
NM_173636.5:c.3210C>G
|
NP_775907.4:p.Ser1070=
|
|