ENST00000450892.7:c.4554T>G
(STRC)
MANE Select
|
ENSP00000401513.2:p.Gly1518=
|
|
ENST00000411560.1:n.142+2010A>C
(CKMT1B)
|
|
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ENST00000428650.5:c.*1587T>G
(STRC)
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ENSP00000415991.1:n.*1587T>G
|
|
ENST00000440125.5:c.*2346T>G
(STRC)
|
ENSP00000394866.1:n.*2346T>G
|
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ENST00000448437.6:n.1674T>G
(STRC)
|
|
|
ENST00000450892.6:c.4554T>G
(STRC)
|
ENSP00000401513.2:p.Gly1518=
|
|
ENST00000460952.1:n.133T>G
(STRC)
|
|
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ENST00000471703.5:n.2508T>G
(STRC)
|
|
|
ENST00000485556.5:n.3409T>G
(STRC)
|
|
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ENST00000493750.1:n.350T>G
(STRC)
|
|
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ENST00000541030.5:c.2235T>G
(STRC)
|
ENSP00000440413.1:p.Gly745=
|
|
NM_153700.2:c.4554T>G
(STRC)
MANE Select
|
NP_714544.1:p.Gly1518=
|
|
XM_011521277.1:c.5043T>G
(STRC)
|
XP_011519579.1:p.Gly1681=
|
|
XM_011521278.1:c.4659T>G
(STRC)
|
XP_011519580.1:p.Gly1553=
|
|
XM_011521279.1:c.4659T>G
(STRC)
|
XP_011519581.1:p.Gly1553=
|
|