ENST00000450892.7:c.4978A>G
(STRC)
MANE Select
|
ENSP00000401513.2:p.Ile1660Val
|
|
ENST00000411560.1:n.142+1016T>C
(CKMT1B)
|
|
|
ENST00000428650.5:c.*2011A>G
(STRC)
|
ENSP00000415991.1:n.*2011A>G
|
|
ENST00000440125.5:c.*2770A>G
(STRC)
|
ENSP00000394866.1:n.*2770A>G
|
|
ENST00000448437.6:n.2098A>G
(STRC)
|
|
|
ENST00000450892.6:c.4978A>G
(STRC)
|
ENSP00000401513.2:p.Ile1660Val
|
|
ENST00000471703.5:n.2932A>G
(STRC)
|
|
|
ENST00000485556.5:n.3833A>G
(STRC)
|
|
|
ENST00000541030.5:c.2659A>G
(STRC)
|
ENSP00000440413.1:p.Ile887Val
|
|
NM_153700.2:c.4978A>G
(STRC)
MANE Select
|
NP_714544.1:p.Ile1660Val
|
|
XM_011521277.1:c.5467A>G
(STRC)
|
XP_011519579.1:p.Ile1823Val
|
|
XM_011521278.1:c.5083A>G
(STRC)
|
XP_011519580.1:p.Ile1695Val
|
|
XM_011521279.1:c.5083A>G
(STRC)
|
XP_011519581.1:p.Ile1695Val
|
|