ENST00000450892.7:c.4127G>C
(STRC)
MANE Select
|
ENSP00000401513.2:p.Gly1376Ala
|
|
ENST00000411560.1:n.143-134C>G
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1330G>C
(STRC)
|
ENSP00000415991.1:n.*1330G>C
|
|
ENST00000440125.5:c.*1919G>C
(STRC)
|
ENSP00000394866.1:n.*1919G>C
|
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ENST00000448437.6:n.1666-3099G>C
(STRC)
|
|
|
ENST00000450892.6:c.4127G>C
(STRC)
|
ENSP00000401513.2:p.Gly1376Ala
|
|
ENST00000471703.5:n.2081G>C
(STRC)
|
|
|
ENST00000485556.5:n.2982G>C
(STRC)
|
|
|
ENST00000541030.5:c.1808G>C
(STRC)
|
ENSP00000440413.1:p.Gly603Ala
|
|
NM_153700.2:c.4127G>C
(STRC)
MANE Select
|
NP_714544.1:p.Gly1376Ala
|
|
XM_011521277.1:c.4616G>C
(STRC)
|
XP_011519579.1:p.Gly1539Ala
|
|
XM_011521278.1:c.4232G>C
(STRC)
|
XP_011519580.1:p.Gly1411Ala
|
|
XM_011521279.1:c.4232G>C
(STRC)
|
XP_011519581.1:p.Gly1411Ala
|
|