ENST00000450892.7:c.4045C>G
(STRC)
MANE Select
|
ENSP00000401513.2:p.Leu1349Val
|
|
ENST00000411560.1:n.143-52G>C
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1248C>G
(STRC)
|
ENSP00000415991.1:n.*1248C>G
|
|
ENST00000440125.5:c.*1837C>G
(STRC)
|
ENSP00000394866.1:n.*1837C>G
|
|
ENST00000448437.6:n.1665+3131C>G
(STRC)
|
|
|
ENST00000450892.6:c.4045C>G
(STRC)
|
ENSP00000401513.2:p.Leu1349Val
|
|
ENST00000455136.5:c.1076C>G
(STRC)
|
|
|
ENST00000471703.5:n.1999C>G
(STRC)
|
|
|
ENST00000485556.5:n.2900C>G
(STRC)
|
|
|
ENST00000541030.5:c.1726C>G
(STRC)
|
ENSP00000440413.1:p.Leu576Val
|
|
NM_153700.2:c.4045C>G
(STRC)
MANE Select
|
NP_714544.1:p.Leu1349Val
|
|
XM_011521277.1:c.4534C>G
(STRC)
|
XP_011519579.1:p.Leu1512Val
|
|
XM_011521278.1:c.4150C>G
(STRC)
|
XP_011519580.1:p.Leu1384Val
|
|
XM_011521279.1:c.4150C>G
(STRC)
|
XP_011519581.1:p.Leu1384Val
|
|