ENST00000450892.7:c.4970T>C
(STRC)
MANE Select
|
ENSP00000401513.2:p.Phe1657Ser
|
|
ENST00000411560.1:n.142+1024A>G
(CKMT1B)
|
|
|
ENST00000428650.5:c.*2003T>C
(STRC)
|
ENSP00000415991.1:n.*2003T>C
|
|
ENST00000440125.5:c.*2762T>C
(STRC)
|
ENSP00000394866.1:n.*2762T>C
|
|
ENST00000448437.6:n.2090T>C
(STRC)
|
|
|
ENST00000450892.6:c.4970T>C
(STRC)
|
ENSP00000401513.2:p.Phe1657Ser
|
|
ENST00000471703.5:n.2924T>C
(STRC)
|
|
|
ENST00000485556.5:n.3825T>C
(STRC)
|
|
|
ENST00000541030.5:c.2651T>C
(STRC)
|
ENSP00000440413.1:p.Phe884Ser
|
|
NM_153700.2:c.4970T>C
(STRC)
MANE Select
|
NP_714544.1:p.Phe1657Ser
|
|
XM_011521277.1:c.5459T>C
(STRC)
|
XP_011519579.1:p.Phe1820Ser
|
|
XM_011521278.1:c.5075T>C
(STRC)
|
XP_011519580.1:p.Phe1692Ser
|
|
XM_011521279.1:c.5075T>C
(STRC)
|
XP_011519581.1:p.Phe1692Ser
|
|