ENST00000450892.7:c.4549T>G
(STRC)
MANE Select
|
ENSP00000401513.2:p.Trp1517Gly
|
|
ENST00000411560.1:n.142+2015A>C
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1582T>G
(STRC)
|
ENSP00000415991.1:n.*1582T>G
|
|
ENST00000440125.5:c.*2341T>G
(STRC)
|
ENSP00000394866.1:n.*2341T>G
|
|
ENST00000448437.6:n.1669T>G
(STRC)
|
|
|
ENST00000450892.6:c.4549T>G
(STRC)
|
ENSP00000401513.2:p.Trp1517Gly
|
|
ENST00000460952.1:n.128T>G
(STRC)
|
|
|
ENST00000471703.5:n.2503T>G
(STRC)
|
|
|
ENST00000485556.5:n.3404T>G
(STRC)
|
|
|
ENST00000493750.1:n.345T>G
(STRC)
|
|
|
ENST00000541030.5:c.2230T>G
(STRC)
|
ENSP00000440413.1:p.Trp744Gly
|
|
NM_153700.2:c.4549T>G
(STRC)
MANE Select
|
NP_714544.1:p.Trp1517Gly
|
|
XM_011521277.1:c.5038T>G
(STRC)
|
XP_011519579.1:p.Trp1680Gly
|
|
XM_011521278.1:c.4654T>G
(STRC)
|
XP_011519580.1:p.Trp1552Gly
|
|
XM_011521279.1:c.4654T>G
(STRC)
|
XP_011519581.1:p.Trp1552Gly
|
|