|
ENST00000427738.8:c.2803G>T
(CYLD)
MANE Select
|
ENSP00000392025.3:p.Ala935Ser
|
|
|
ENST00000311559.13:c.2803G>T
(CYLD)
|
ENSP00000308928.9:p.Ala935Ser
|
|
|
ENST00000398568.6:c.2794G>T
(CYLD)
|
ENSP00000381574.2:p.Ala932Ser
|
|
|
ENST00000427738.7:c.2803G>T
(CYLD)
|
ENSP00000392025.3:p.Ala935Ser
|
|
|
ENST00000564326.5:c.2794G>T
(CYLD)
|
ENSP00000454515.1:p.Ala932Ser
|
|
|
ENST00000566024.1:c.177+1970G>T
(CYLD)
|
|
|
|
ENST00000568704.2:c.2248G>T
(CYLD)
|
ENSP00000456488.2:p.Ala750Ser
|
|
|
ENST00000569418.5:c.2794G>T
(CYLD)
|
ENSP00000457576.1:p.Ala932Ser
|
|
|
NM_001042355.1:c.2794G>T
(CYLD)
|
NP_001035814.1:p.Ala932Ser
|
|
|
NM_001042412.1:c.2794G>T
(CYLD)
|
NP_001035877.1:p.Ala932Ser
|
|
|
NM_015247.2:c.2803G>T , LRG_491t1:c.2803G>T
(CYLD)
|
NP_056062.1:p.Ala935Ser
|
|
|
XM_005255812.2:c.2794G>T
(CYLD)
|
XP_005255869.1:p.Ala932Ser
|
|
|
XM_006721149.1:c.2794G>T
(CYLD)
|
XP_006721212.1:p.Ala932Ser
|
|
|
XM_011522906.1:c.2794G>T
(CYLD)
|
XP_011521208.1:p.Ala932Ser
|
|
|
XM_011522907.1:c.2794G>T
(CYLD)
|
XP_011521209.1:p.Ala932Ser
|
|
|
XM_011522908.1:c.2764G>T
(CYLD)
|
XP_011521210.1:p.Ala922Ser
|
|
|
XM_011522909.1:c.2677+2012G>T
(CYLD)
|
XP_011521211.1:n.2677+2012G>T
|
|
|
XM_011522910.1:c.2677+2012G>T
(CYLD)
|
XP_011521212.1:n.2677+2012G>T
|
|
|
XR_933218.1:n.3087G>T
(CYLD)
|
|
|
|
XR_933542.1:n.2450+5683C>A
(CYLD-AS2)
|
|
|
|
XM_011522907.2:c.2794G>T
(CYLD)
|
XP_011521209.1:p.Ala932Ser
|
|
|
XM_017022977.1:c.2794G>T
(CYLD)
|
XP_016878466.1:p.Ala932Ser
|
|
|
XM_017022978.1:c.2794G>T
(CYLD)
|
XP_016878467.1:p.Ala932Ser
|
|
|
XM_017022979.1:c.2794G>T
(CYLD)
|
XP_016878468.1:p.Ala932Ser
|
|
|
XM_017022980.1:c.2794G>T
(CYLD)
|
XP_016878469.1:p.Ala932Ser
|
|
|
XM_017022981.2:c.2764G>T
(CYLD)
|
XP_016878470.1:p.Ala922Ser
|
|
|
XR_001751849.1:n.2921G>T
(CYLD)
|
|
|
|
XR_933542.2:n.4187+5683C>A
(CYLD-AS2)
|
|
|
|
NM_001042355.2:c.2794G>T
(CYLD)
|
NP_001035814.1:p.Ala932Ser
|
|
|
NM_001042412.2:c.2794G>T
(CYLD)
|
NP_001035877.1:p.Ala932Ser
|
|
|
NM_001042412.3:c.2794G>T
(CYLD)
|
NP_001035877.1:p.Ala932Ser
|
|
|
NM_001378743.1:c.2803G>T
(CYLD)
MANE Select
|
NP_001365672.1:p.Ala935Ser
|
|
|
NM_001378744.1:c.2794G>T
(CYLD)
|
NP_001365673.1:p.Ala932Ser
|
|
|
NM_001378745.1:c.2794G>T
(CYLD)
|
NP_001365674.1:p.Ala932Ser
|
|
|
NM_001378746.1:c.2794G>T
(CYLD)
|
NP_001365675.1:p.Ala932Ser
|
|
|
NM_001378747.1:c.2794G>T
(CYLD)
|
NP_001365676.1:p.Ala932Ser
|
|
|
NM_001378748.1:c.2794G>T
(CYLD)
|
NP_001365677.1:p.Ala932Ser
|
|
|
NM_001378749.1:c.2794G>T
(CYLD)
|
NP_001365678.1:p.Ala932Ser
|
|
|
NM_001378750.1:c.2794G>T
(CYLD)
|
NP_001365679.1:p.Ala932Ser
|
|
|
NM_001378751.1:c.2764G>T
(CYLD)
|
NP_001365680.1:p.Ala922Ser
|
|
|
NM_001378752.1:c.2764G>T
(CYLD)
|
NP_001365681.1:p.Ala922Ser
|
|
|
NM_001378753.1:c.2764G>T
(CYLD)
|
NP_001365682.1:p.Ala922Ser
|
|
|
NM_001378754.1:c.2128G>T
(CYLD)
|
NP_001365683.1:p.Ala710Ser
|
|
|
NM_001378755.1:c.2128G>T
(CYLD)
|
NP_001365684.1:p.Ala710Ser
|
|
|
NM_015247.3:c.2803G>T
(CYLD)
|
NP_056062.1:p.Ala935Ser
|
|
|
NR_166071.1:n.2892G>T
(CYLD)
|
|
|
