ENST00000270301.12:c.4167T>A
|
ENSP00000270301.6:p.Pro1389=
|
|
ENST00000401500.7:c.4182T>A
MANE Select
|
ENSP00000384792.1:p.Pro1394=
|
|
ENST00000587391.6:c.*4042T>A
|
ENSP00000465525.1:n.*4042T>A
|
|
ENST00000679357.1:c.2262T>A
|
|
|
ENST00000679598.1:c.927T>A
|
|
|
ENST00000679682.1:c.4167T>A
|
ENSP00000506226.1:p.Pro1389=
|
|
ENST00000679714.1:c.4176T>A
|
ENSP00000506627.1:p.Pro1392=
|
|
ENST00000679757.1:c.3831T>A
|
ENSP00000505158.1:p.Pro1277=
|
|
ENST00000679858.1:c.*3564T>A
|
ENSP00000505655.1:n.*3564T>A
|
|
ENST00000680211.1:c.783T>A
|
ENSP00000506102.1:p.Pro261=
|
|
ENST00000680280.1:n.1685T>A
|
|
|
ENST00000680349.1:n.2831T>A
|
|
|
ENST00000680403.1:c.4167T>A
|
ENSP00000505677.1:p.Pro1389=
|
|
ENST00000680564.1:c.3933T>A
|
ENSP00000505582.1:p.Pro1311=
|
|
ENST00000680590.1:c.*2562T>A
|
ENSP00000505350.1:n.*2562T>A
|
|
ENST00000680597.1:c.915T>A
|
|
|
ENST00000680739.1:c.1197T>A
|
|
|
ENST00000680773.1:n.2683T>A
|
|
|
ENST00000680806.1:c.*3485T>A
|
ENSP00000506418.1:n.*3485T>A
|
|
ENST00000680997.1:n.2114T>A
|
|
|
ENST00000681608.1:n.2027T>A
|
|
|
ENST00000681625.1:c.*1514T>A
|
ENSP00000505555.1:n.*1514T>A
|
|
ENST00000681648.1:n.2233T>A
|
|
|
ENST00000270301.11:c.4167T>A
|
ENSP00000270301.6:p.Pro1389=
|
|
ENST00000401500.6:c.4182T>A
|
ENSP00000384792.1:p.Pro1394=
|
|
ENST00000587391.5:c.*4042T>A
|
ENSP00000465525.1:n.*4042T>A
|
|
NM_001083961.1:c.4182T>A
|
NP_001077430.1:p.Pro1394=
|
|
NM_173636.4:c.4167T>A
|
NP_775907.4:p.Pro1389=
|
|
XM_005258809.2:c.4071T>A
|
XP_005258866.1:p.Pro1357=
|
|
XM_011526837.1:c.4167T>A
|
XP_011525139.1:p.Pro1389=
|
|
XM_011526838.1:c.3933T>A
|
XP_011525140.1:p.Pro1311=
|
|
XM_011526839.1:c.3831T>A
|
XP_011525141.1:p.Pro1277=
|
|
XM_011526840.1:c.3174T>A
|
XP_011525142.1:p.Pro1058=
|
|
XM_011526841.1:c.2760T>A
|
XP_011525143.1:p.Pro920=
|
|
XM_011526842.1:c.2613T>A
|
XP_011525144.1:p.Pro871=
|
|
XM_011526843.1:c.1929T>A
|
XP_011525145.1:p.Pro643=
|
|
XM_011526844.1:c.1929T>A
|
XP_011525146.1:p.Pro643=
|
|
XM_011526840.2:c.3174T>A
|
XP_011525142.1:p.Pro1058=
|
|
XM_011526841.2:c.2760T>A
|
XP_011525143.1:p.Pro920=
|
|
XM_011526844.2:c.1929T>A
|
XP_011525146.1:p.Pro643=
|
|
XM_017026665.1:c.4182T>A
|
XP_016882154.1:p.Pro1394=
|
|
NM_001083961.2:c.4182T>A
MANE Select
|
NP_001077430.1:p.Pro1394=
|
|
NM_173636.5:c.4167T>A
|
NP_775907.4:p.Pro1389=
|
|