ENST00000270301.12:c.4218C>T
|
ENSP00000270301.6:p.Pro1406=
|
|
ENST00000401500.7:c.4233C>T
MANE Select
|
ENSP00000384792.1:p.Pro1411=
|
|
ENST00000587391.6:c.*4093C>T
|
ENSP00000465525.1:n.*4093C>T
|
|
ENST00000679357.1:c.2313C>T
|
|
|
ENST00000679598.1:c.978C>T
|
|
|
ENST00000679682.1:c.4218C>T
|
ENSP00000506226.1:p.Pro1406=
|
|
ENST00000679714.1:c.4227C>T
|
ENSP00000506627.1:p.Pro1409=
|
|
ENST00000679757.1:c.3882C>T
|
ENSP00000505158.1:p.Pro1294=
|
|
ENST00000679858.1:c.*3615C>T
|
ENSP00000505655.1:n.*3615C>T
|
|
ENST00000680211.1:c.834C>T
|
ENSP00000506102.1:p.Pro278=
|
|
ENST00000680280.1:n.1736C>T
|
|
|
ENST00000680349.1:n.2882C>T
|
|
|
ENST00000680403.1:c.4218C>T
|
ENSP00000505677.1:p.Pro1406=
|
|
ENST00000680564.1:c.3984C>T
|
ENSP00000505582.1:p.Pro1328=
|
|
ENST00000680590.1:c.*2613C>T
|
ENSP00000505350.1:n.*2613C>T
|
|
ENST00000680597.1:c.966C>T
|
|
|
ENST00000680739.1:c.1248C>T
|
|
|
ENST00000680773.1:n.2734C>T
|
|
|
ENST00000680806.1:c.*3536C>T
|
ENSP00000506418.1:n.*3536C>T
|
|
ENST00000680997.1:n.2165C>T
|
|
|
ENST00000681608.1:n.2078C>T
|
|
|
ENST00000681625.1:c.*1565C>T
|
ENSP00000505555.1:n.*1565C>T
|
|
ENST00000681648.1:n.2284C>T
|
|
|
ENST00000270301.11:c.4218C>T
|
ENSP00000270301.6:p.Pro1406=
|
|
ENST00000401500.6:c.4233C>T
|
ENSP00000384792.1:p.Pro1411=
|
|
ENST00000587391.5:c.*4093C>T
|
ENSP00000465525.1:n.*4093C>T
|
|
NM_001083961.1:c.4233C>T
|
NP_001077430.1:p.Pro1411=
|
|
NM_173636.4:c.4218C>T
|
NP_775907.4:p.Pro1406=
|
|
XM_005258809.2:c.4122C>T
|
XP_005258866.1:p.Pro1374=
|
|
XM_011526837.1:c.4218C>T
|
XP_011525139.1:p.Pro1406=
|
|
XM_011526838.1:c.3984C>T
|
XP_011525140.1:p.Pro1328=
|
|
XM_011526839.1:c.3882C>T
|
XP_011525141.1:p.Pro1294=
|
|
XM_011526840.1:c.3225C>T
|
XP_011525142.1:p.Pro1075=
|
|
XM_011526841.1:c.2811C>T
|
XP_011525143.1:p.Pro937=
|
|
XM_011526842.1:c.2664C>T
|
XP_011525144.1:p.Pro888=
|
|
XM_011526843.1:c.1980C>T
|
XP_011525145.1:p.Pro660=
|
|
XM_011526844.1:c.1980C>T
|
XP_011525146.1:p.Pro660=
|
|
XM_011526840.2:c.3225C>T
|
XP_011525142.1:p.Pro1075=
|
|
XM_011526841.2:c.2811C>T
|
XP_011525143.1:p.Pro937=
|
|
XM_011526844.2:c.1980C>T
|
XP_011525146.1:p.Pro660=
|
|
XM_017026665.1:c.4233C>T
|
XP_016882154.1:p.Pro1411=
|
|
NM_001083961.2:c.4233C>T
MANE Select
|
NP_001077430.1:p.Pro1411=
|
|
NM_173636.5:c.4218C>T
|
NP_775907.4:p.Pro1406=
|
|