ENST00000450892.7:c.4186C>G
(STRC)
MANE Select
|
ENSP00000401513.2:p.Leu1396Val
|
|
ENST00000411560.1:n.143-391G>C
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1389C>G
(STRC)
|
ENSP00000415991.1:n.*1389C>G
|
|
ENST00000440125.5:c.*1978C>G
(STRC)
|
ENSP00000394866.1:n.*1978C>G
|
|
ENST00000448437.6:n.1666-2842C>G
(STRC)
|
|
|
ENST00000450892.6:c.4186C>G
(STRC)
|
ENSP00000401513.2:p.Leu1396Val
|
|
ENST00000471703.5:n.2140C>G
(STRC)
|
|
|
ENST00000485556.5:n.3041C>G
(STRC)
|
|
|
ENST00000541030.5:c.1867C>G
(STRC)
|
ENSP00000440413.1:p.Leu623Val
|
|
NM_153700.2:c.4186C>G
(STRC)
MANE Select
|
NP_714544.1:p.Leu1396Val
|
|
XM_011521277.1:c.4675C>G
(STRC)
|
XP_011519579.1:p.Leu1559Val
|
|
XM_011521278.1:c.4291C>G
(STRC)
|
XP_011519580.1:p.Leu1431Val
|
|
XM_011521279.1:c.4291C>G
(STRC)
|
XP_011519581.1:p.Leu1431Val
|
|