|
ENST00000450892.7:c.4561_4562delinsCG
(STRC)
MANE Select
|
ENSP00000401513.2:p.Arg1521=
|
|
|
ENST00000411560.1:n.142+2002_142+2003delinsCG
(CKMT1B)
|
|
|
|
ENST00000428650.5:c.*1594_*1595delinsCG
(STRC)
|
ENSP00000415991.1:n.*1594_*1595delinsCG
|
|
|
ENST00000440125.5:c.*2353_*2354delinsCG
(STRC)
|
ENSP00000394866.1:n.*2353_*2354delinsCG
|
|
|
ENST00000448437.6:n.1681_1682delinsCG
(STRC)
|
|
|
|
ENST00000450892.6:c.4561_4562delinsCG
(STRC)
|
ENSP00000401513.2:p.Arg1521=
|
|
|
ENST00000460952.1:n.140_141delinsCG
(STRC)
|
|
|
|
ENST00000471703.5:n.2515_2516delinsCG
(STRC)
|
|
|
|
ENST00000485556.5:n.3416_3417delinsCG
(STRC)
|
|
|
|
ENST00000493750.1:n.357_358delinsCG
(STRC)
|
|
|
|
ENST00000541030.5:c.2242_2243delinsCG
(STRC)
|
ENSP00000440413.1:p.Arg748=
|
|
|
NM_153700.2:c.4561_4562delinsCG
(STRC)
MANE Select
|
NP_714544.1:p.Arg1521=
|
|
|
XM_011521277.1:c.5050_5051delinsCG
(STRC)
|
XP_011519579.1:p.Arg1684=
|
|
|
XM_011521278.1:c.4666_4667delinsCG
(STRC)
|
XP_011519580.1:p.Arg1556=
|
|
|
XM_011521279.1:c.4666_4667delinsCG
(STRC)
|
XP_011519581.1:p.Arg1556=
|
|
