ENST00000450892.7:c.4906C>G
(STRC)
MANE Select
|
ENSP00000401513.2:p.Leu1636Val
|
|
ENST00000411560.1:n.142+1088G>C
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1939C>G
(STRC)
|
ENSP00000415991.1:n.*1939C>G
|
|
ENST00000440125.5:c.*2698C>G
(STRC)
|
ENSP00000394866.1:n.*2698C>G
|
|
ENST00000448437.6:n.2026C>G
(STRC)
|
|
|
ENST00000450892.6:c.4906C>G
(STRC)
|
ENSP00000401513.2:p.Leu1636Val
|
|
ENST00000460952.1:n.485C>G
(STRC)
|
|
|
ENST00000471703.5:n.2860C>G
(STRC)
|
|
|
ENST00000485556.5:n.3761C>G
(STRC)
|
|
|
ENST00000541030.5:c.2587C>G
(STRC)
|
ENSP00000440413.1:p.Leu863Val
|
|
NM_153700.2:c.4906C>G
(STRC)
MANE Select
|
NP_714544.1:p.Leu1636Val
|
|
XM_011521277.1:c.5395C>G
(STRC)
|
XP_011519579.1:p.Leu1799Val
|
|
XM_011521278.1:c.5011C>G
(STRC)
|
XP_011519580.1:p.Leu1671Val
|
|
XM_011521279.1:c.5011C>G
(STRC)
|
XP_011519581.1:p.Leu1671Val
|
|