ENST00000270301.12:c.3240C=
|
ENSP00000270301.6:p.Ala1080=
|
|
ENST00000401500.7:c.3255C=
MANE Select
|
ENSP00000384792.1:p.Ala1085=
|
|
ENST00000587391.6:c.*3115C=
|
ENSP00000465525.1:n.*3115C=
|
|
ENST00000679357.1:c.1335C=
|
|
|
ENST00000679598.1:c.20C=
|
|
|
ENST00000679682.1:c.3240C=
|
ENSP00000506226.1:p.Ala1080=
|
|
ENST00000679714.1:c.3249C=
|
ENSP00000506627.1:p.Ala1083=
|
|
ENST00000679757.1:c.2904C=
|
ENSP00000505158.1:p.Ala968=
|
|
ENST00000679858.1:c.*2637C=
|
ENSP00000505655.1:n.*2637C=
|
|
ENST00000680211.1:c.-145C=
|
ENSP00000506102.1:n.-145C=
|
|
ENST00000680280.1:n.542C=
|
|
|
ENST00000680349.1:n.1823C=
|
|
|
ENST00000680403.1:c.3240C=
|
ENSP00000505677.1:p.Ala1080=
|
|
ENST00000680564.1:c.3006C=
|
ENSP00000505582.1:p.Ala1002=
|
|
ENST00000680590.1:c.*1635C=
|
ENSP00000505350.1:n.*1635C=
|
|
ENST00000680597.1:c.20C=
|
|
|
ENST00000680739.1:c.270C=
|
|
|
ENST00000680773.1:n.1756C=
|
|
|
ENST00000680806.1:c.*2558C=
|
ENSP00000506418.1:n.*2558C=
|
|
ENST00000680997.1:n.1187C=
|
|
|
ENST00000681608.1:n.788C=
|
|
|
ENST00000681625.1:c.*587C=
|
ENSP00000505555.1:n.*587C=
|
|
ENST00000681648.1:n.554C=
|
|
|
ENST00000270301.11:c.3240C=
|
ENSP00000270301.6:p.Ala1080=
|
|
ENST00000401500.6:c.3255C=
|
ENSP00000384792.1:p.Ala1085=
|
|
ENST00000587391.5:c.*3115C=
|
ENSP00000465525.1:n.*3115C=
|
|
NM_001083961.1:c.3255C=
|
NP_001077430.1:p.Ala1085=
|
|
NM_173636.4:c.3240C=
|
NP_775907.4:p.Ala1080=
|
|
XM_005258809.2:c.3144C=
|
XP_005258866.1:p.Ala1048=
|
|
XM_011526837.1:c.3240C=
|
XP_011525139.1:p.Ala1080=
|
|
XM_011526838.1:c.3006C=
|
XP_011525140.1:p.Ala1002=
|
|
XM_011526839.1:c.2904C=
|
XP_011525141.1:p.Ala968=
|
|
XM_011526840.1:c.2247C=
|
XP_011525142.1:p.Ala749=
|
|
XM_011526841.1:c.1833C=
|
XP_011525143.1:p.Ala611=
|
|
XM_011526842.1:c.1686C=
|
XP_011525144.1:p.Ala562=
|
|
XM_011526843.1:c.1002C=
|
XP_011525145.1:p.Ala334=
|
|
XM_011526844.1:c.1002C=
|
XP_011525146.1:p.Ala334=
|
|
XM_011526840.2:c.2247C=
|
XP_011525142.1:p.Ala749=
|
|
XM_011526841.2:c.1833C=
|
XP_011525143.1:p.Ala611=
|
|
XM_011526844.2:c.1002C=
|
XP_011525146.1:p.Ala334=
|
|
XM_017026665.1:c.3255C=
|
XP_016882154.1:p.Ala1085=
|
|
NM_001083961.2:c.3255C=
MANE Select
|
NP_001077430.1:p.Ala1085=
|
|
NM_173636.5:c.3240C=
|
NP_775907.4:p.Ala1080=
|
|