ENST00000270301.12:c.3093T>C
|
ENSP00000270301.6:p.Gly1031=
|
|
ENST00000401500.7:c.3093T>C
MANE Select
|
ENSP00000384792.1:p.Gly1031=
|
|
ENST00000587391.6:c.*2368T>C
|
ENSP00000465525.1:n.*2368T>C
|
|
ENST00000679357.1:c.883T>C
|
|
|
ENST00000679422.1:c.772T>C
|
|
|
ENST00000679682.1:c.3078T>C
|
ENSP00000506226.1:p.Gly1026=
|
|
ENST00000679714.1:c.3087T>C
|
ENSP00000506627.1:p.Gly1029=
|
|
ENST00000679757.1:c.2742T>C
|
ENSP00000505158.1:p.Gly914=
|
|
ENST00000679858.1:c.*2475T>C
|
ENSP00000505655.1:n.*2475T>C
|
|
ENST00000680211.1:c.-307T>C
|
ENSP00000506102.1:n.-307T>C
|
|
ENST00000680349.1:n.1076T>C
|
|
|
ENST00000680403.1:c.3093T>C
|
ENSP00000505677.1:p.Gly1031=
|
|
ENST00000680564.1:c.2971+707T>C
|
ENSP00000505582.1:n.2971+707T>C
|
|
ENST00000680590.1:c.*1488T>C
|
ENSP00000505350.1:n.*1488T>C
|
|
ENST00000680739.1:c.11T>C
|
|
|
ENST00000680773.1:n.1009T>C
|
|
|
ENST00000680806.1:c.*1811T>C
|
ENSP00000506418.1:n.*1811T>C
|
|
ENST00000680997.1:n.440T>C
|
|
|
ENST00000681088.1:c.755T>C
|
|
|
ENST00000681608.1:n.41T>C
|
|
|
ENST00000681625.1:c.*425T>C
|
ENSP00000505555.1:n.*425T>C
|
|
ENST00000270301.11:c.3093T>C
|
ENSP00000270301.6:p.Gly1031=
|
|
ENST00000401500.6:c.3093T>C
|
ENSP00000384792.1:p.Gly1031=
|
|
ENST00000587391.5:c.*2368T>C
|
ENSP00000465525.1:n.*2368T>C
|
|
NM_001083961.1:c.3093T>C
|
NP_001077430.1:p.Gly1031=
|
|
NM_173636.4:c.3093T>C
|
NP_775907.4:p.Gly1031=
|
|
XM_005258809.2:c.2982T>C
|
XP_005258866.1:p.Gly994=
|
|
XM_011526837.1:c.3078T>C
|
XP_011525139.1:p.Gly1026=
|
|
XM_011526838.1:c.2971+707T>C
|
XP_011525140.1:n.2971+707T>C
|
|
XM_011526839.1:c.2742T>C
|
XP_011525141.1:p.Gly914=
|
|
XM_011526840.1:c.2085T>C
|
XP_011525142.1:p.Gly695=
|
|
XM_011526841.1:c.1671T>C
|
XP_011525143.1:p.Gly557=
|
|
XM_011526842.1:c.1524T>C
|
XP_011525144.1:p.Gly508=
|
|
XM_011526843.1:c.840T>C
|
XP_011525145.1:p.Gly280=
|
|
XM_011526844.1:c.840T>C
|
XP_011525146.1:p.Gly280=
|
|
XM_011526840.2:c.2085T>C
|
XP_011525142.1:p.Gly695=
|
|
XM_011526841.2:c.1671T>C
|
XP_011525143.1:p.Gly557=
|
|
XM_011526844.2:c.840T>C
|
XP_011525146.1:p.Gly280=
|
|
XM_017026665.1:c.3093T>C
|
XP_016882154.1:p.Gly1031=
|
|
NM_001083961.2:c.3093T>C
MANE Select
|
NP_001077430.1:p.Gly1031=
|
|
NM_173636.5:c.3093T>C
|
NP_775907.4:p.Gly1031=
|
|