ENST00000450892.7:c.4399G>A
(STRC)
MANE Select
|
ENSP00000401513.2:p.Val1467Ile
|
|
ENST00000411560.1:n.143-1396C>T
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1578+608G>A
(STRC)
|
ENSP00000415991.1:n.*1578+608G>A
|
|
ENST00000440125.5:c.*2191G>A
(STRC)
|
ENSP00000394866.1:n.*2191G>A
|
|
ENST00000448437.6:n.1666-1837G>A
(STRC)
|
|
|
ENST00000450892.6:c.4399G>A
(STRC)
|
ENSP00000401513.2:p.Val1467Ile
|
|
ENST00000471703.5:n.2353G>A
(STRC)
|
|
|
ENST00000485556.5:n.3254G>A
(STRC)
|
|
|
ENST00000493750.1:n.195G>A
(STRC)
|
|
|
ENST00000541030.5:c.2080G>A
(STRC)
|
ENSP00000440413.1:p.Val694Ile
|
|
NM_153700.2:c.4399G>A
(STRC)
MANE Select
|
NP_714544.1:p.Val1467Ile
|
|
XM_011521277.1:c.4888G>A
(STRC)
|
XP_011519579.1:p.Val1630Ile
|
|
XM_011521278.1:c.4504G>A
(STRC)
|
XP_011519580.1:p.Val1502Ile
|
|
XM_011521279.1:c.4504G>A
(STRC)
|
XP_011519581.1:p.Val1502Ile
|
|