ENST00000270301.12:c.4190T=
|
ENSP00000270301.6:p.Val1397=
|
|
ENST00000401500.7:c.4205T=
MANE Select
|
ENSP00000384792.1:p.Val1402=
|
|
ENST00000587391.6:c.*4065T=
|
ENSP00000465525.1:n.*4065T=
|
|
ENST00000679357.1:c.2285T=
|
|
|
ENST00000679598.1:c.950T=
|
|
|
ENST00000679682.1:c.4190T=
|
ENSP00000506226.1:p.Val1397=
|
|
ENST00000679714.1:c.4199T=
|
ENSP00000506627.1:p.Val1400=
|
|
ENST00000679757.1:c.3854T=
|
ENSP00000505158.1:p.Val1285=
|
|
ENST00000679858.1:c.*3587T=
|
ENSP00000505655.1:n.*3587T=
|
|
ENST00000680211.1:c.806T=
|
ENSP00000506102.1:p.Val269=
|
|
ENST00000680280.1:n.1708T=
|
|
|
ENST00000680349.1:n.2854T=
|
|
|
ENST00000680403.1:c.4190T=
|
ENSP00000505677.1:p.Val1397=
|
|
ENST00000680564.1:c.3956T=
|
ENSP00000505582.1:p.Val1319=
|
|
ENST00000680590.1:c.*2585T=
|
ENSP00000505350.1:n.*2585T=
|
|
ENST00000680597.1:c.938T=
|
|
|
ENST00000680739.1:c.1220T=
|
|
|
ENST00000680773.1:n.2706T=
|
|
|
ENST00000680806.1:c.*3508T=
|
ENSP00000506418.1:n.*3508T=
|
|
ENST00000680997.1:n.2137T=
|
|
|
ENST00000681608.1:n.2050T=
|
|
|
ENST00000681625.1:c.*1537T=
|
ENSP00000505555.1:n.*1537T=
|
|
ENST00000681648.1:n.2256T=
|
|
|
ENST00000270301.11:c.4190T=
|
ENSP00000270301.6:p.Val1397=
|
|
ENST00000401500.6:c.4205T=
|
ENSP00000384792.1:p.Val1402=
|
|
ENST00000587391.5:c.*4065T=
|
ENSP00000465525.1:n.*4065T=
|
|
NM_001083961.1:c.4205T=
|
NP_001077430.1:p.Val1402=
|
|
NM_173636.4:c.4190T=
|
NP_775907.4:p.Val1397=
|
|
XM_005258809.2:c.4094T=
|
XP_005258866.1:p.Val1365=
|
|
XM_011526837.1:c.4190T=
|
XP_011525139.1:p.Val1397=
|
|
XM_011526838.1:c.3956T=
|
XP_011525140.1:p.Val1319=
|
|
XM_011526839.1:c.3854T=
|
XP_011525141.1:p.Val1285=
|
|
XM_011526840.1:c.3197T=
|
XP_011525142.1:p.Val1066=
|
|
XM_011526841.1:c.2783T=
|
XP_011525143.1:p.Val928=
|
|
XM_011526842.1:c.2636T=
|
XP_011525144.1:p.Val879=
|
|
XM_011526843.1:c.1952T=
|
XP_011525145.1:p.Val651=
|
|
XM_011526844.1:c.1952T=
|
XP_011525146.1:p.Val651=
|
|
XM_011526840.2:c.3197T=
|
XP_011525142.1:p.Val1066=
|
|
XM_011526841.2:c.2783T=
|
XP_011525143.1:p.Val928=
|
|
XM_011526844.2:c.1952T=
|
XP_011525146.1:p.Val651=
|
|
XM_017026665.1:c.4205T=
|
XP_016882154.1:p.Val1402=
|
|
NM_001083961.2:c.4205T=
MANE Select
|
NP_001077430.1:p.Val1402=
|
|
NM_173636.5:c.4190T=
|
NP_775907.4:p.Val1397=
|
|