ENST00000450892.7:c.4127+5G>T
(STRC)
MANE Select
|
ENSP00000401513.2:n.4127+5G>T
|
|
ENST00000411560.1:n.143-139C>A
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1330+5G>T
(STRC)
|
ENSP00000415991.1:n.*1330+5G>T
|
|
ENST00000440125.5:c.*1919+5G>T
(STRC)
|
ENSP00000394866.1:n.*1919+5G>T
|
|
ENST00000448437.6:n.1666-3094G>T
(STRC)
|
|
|
ENST00000450892.6:c.4127+5G>T
(STRC)
|
ENSP00000401513.2:n.4127+5G>T
|
|
ENST00000471703.5:n.2081+5G>T
(STRC)
|
|
|
ENST00000485556.5:n.2982+5G>T
(STRC)
|
|
|
ENST00000541030.5:c.1808+5G>T
(STRC)
|
ENSP00000440413.1:n.1808+5G>T
|
|
NM_153700.2:c.4127+5G>T
(STRC)
MANE Select
|
NP_714544.1:n.4127+5G>T
|
|
XM_011521277.1:c.4616+5G>T
(STRC)
|
XP_011519579.1:n.4616+5G>T
|
|
XM_011521278.1:c.4232+5G>T
(STRC)
|
XP_011519580.1:n.4232+5G>T
|
|
XM_011521279.1:c.4232+5G>T
(STRC)
|
XP_011519581.1:n.4232+5G>T
|
|