|
ENST00000450892.7:c.4565_4566delinsGA
(STRC)
MANE Select
|
ENSP00000401513.2:p.Gly1522=
|
|
|
ENST00000411560.1:n.142+1998_142+1999delinsTC
(CKMT1B)
|
|
|
|
ENST00000428650.5:c.*1598_*1599delinsGA
(STRC)
|
ENSP00000415991.1:n.*1598_*1599delinsGA
|
|
|
ENST00000440125.5:c.*2357_*2358delinsGA
(STRC)
|
ENSP00000394866.1:n.*2357_*2358delinsGA
|
|
|
ENST00000448437.6:n.1685_1686delinsGA
(STRC)
|
|
|
|
ENST00000450892.6:c.4565_4566delinsGA
(STRC)
|
ENSP00000401513.2:p.Gly1522=
|
|
|
ENST00000460952.1:n.144_145delinsGA
(STRC)
|
|
|
|
ENST00000471703.5:n.2519_2520delinsGA
(STRC)
|
|
|
|
ENST00000485556.5:n.3420_3421delinsGA
(STRC)
|
|
|
|
ENST00000493750.1:n.361_362delinsGA
(STRC)
|
|
|
|
ENST00000541030.5:c.2246_2247delinsGA
(STRC)
|
ENSP00000440413.1:p.Gly749=
|
|
|
NM_153700.2:c.4565_4566delinsGA
(STRC)
MANE Select
|
NP_714544.1:p.Gly1522=
|
|
|
XM_011521277.1:c.5054_5055delinsGA
(STRC)
|
XP_011519579.1:p.Gly1685=
|
|
|
XM_011521278.1:c.4670_4671delinsGA
(STRC)
|
XP_011519580.1:p.Gly1557=
|
|
|
XM_011521279.1:c.4670_4671delinsGA
(STRC)
|
XP_011519581.1:p.Gly1557=
|
|
