ENST00000407010.7:c.1186G>T
(CRPPA)
MANE Select
|
ENSP00000385478.2:p.Glu396Ter
|
|
ENST00000674759.1:c.883G>T
(CRPPA)
|
ENSP00000502749.1:p.Glu295Ter
|
|
ENST00000675257.1:c.778G>T
(CRPPA)
|
ENSP00000501664.1:p.Glu260Ter
|
|
ENST00000676325.1:c.883G>T
(CRPPA)
|
ENSP00000502074.1:p.Glu295Ter
|
|
ENST00000399310.3:c.1036G>T
(CRPPA)
|
ENSP00000382249.3:p.Glu346Ter
|
|
ENST00000407010.6:c.1186G>T
(CRPPA)
|
ENSP00000385478.2:p.Glu396Ter
|
|
NM_001101417.3:c.1036G>T
(CRPPA)
|
NP_001094887.1:p.Glu346Ter
|
|
NM_001101426.3:c.1186G>T
(CRPPA)
|
NP_001094896.1:p.Glu396Ter
|
|
NR_038946.1:n.118+5528C>A
(CRPPA-AS1)
|
|
|
NR_038947.1:n.118+5528C>A
(CRPPA-AS1)
|
|
|
XM_006715770.2:c.937G>T
(CRPPA)
|
XP_006715833.1:p.Glu313Ter
|
|
XM_011515497.1:c.1186G>T
(CRPPA)
|
XP_011513799.1:p.Glu396Ter
|
|
XM_011515498.1:c.1186G>T
(CRPPA)
|
XP_011513800.1:p.Glu396Ter
|
|
XM_011515500.1:c.1081G>T
(CRPPA)
|
XP_011513802.1:p.Glu361Ter
|
|
XM_011515502.1:c.883G>T
(CRPPA)
|
XP_011513804.1:p.Glu295Ter
|
|
XM_011515503.1:c.883G>T
(CRPPA)
|
XP_011513805.1:p.Glu295Ter
|
|
XM_011515504.1:c.883G>T
(CRPPA)
|
XP_011513806.1:p.Glu295Ter
|
|
XM_011515505.1:c.883G>T
(CRPPA)
|
XP_011513807.1:p.Glu295Ter
|
|
XM_011515506.1:c.883G>T
(CRPPA)
|
XP_011513808.1:p.Glu295Ter
|
|
XM_011515507.1:c.883G>T
(CRPPA)
|
XP_011513809.1:p.Glu295Ter
|
|
XM_011515508.1:c.883G>T
(CRPPA)
|
XP_011513810.1:p.Glu295Ter
|
|
XM_011515509.1:c.883G>T
(CRPPA)
|
XP_011513811.1:p.Glu295Ter
|
|
XM_006715770.3:c.937G>T
(CRPPA)
|
XP_006715833.1:p.Glu313Ter
|
|
XM_011515500.2:c.1081G>T
(CRPPA)
|
XP_011513802.1:p.Glu361Ter
|
|
XM_011515508.2:c.883G>T
(CRPPA)
|
XP_011513810.1:p.Glu295Ter
|
|
XM_011515509.2:c.883G>T
(CRPPA)
|
XP_011513811.1:p.Glu295Ter
|
|
XM_017012575.1:c.1186G>T
(CRPPA)
|
XP_016868064.1:p.Glu396Ter
|
|
XM_017012577.1:c.550G>T
(CRPPA)
|
XP_016868066.1:p.Glu184Ter
|
|
XM_017012578.1:c.550G>T
(CRPPA)
|
XP_016868067.1:p.Glu184Ter
|
|
XM_024446909.1:c.883G>T
(CRPPA)
|
XP_024302677.1:p.Glu295Ter
|
|
XM_024446910.1:c.883G>T
(CRPPA)
|
XP_024302678.1:p.Glu295Ter
|
|
XM_024446911.1:c.778G>T
(CRPPA)
|
XP_024302679.1:p.Glu260Ter
|
|
XR_001744868.1:n.1194G>T
(CRPPA)
|
|
|
NM_001101426.4:c.1186G>T
(CRPPA)
MANE Select
|
NP_001094896.1:p.Glu396Ter
|
|
NM_001101417.4:c.1036G>T
(CRPPA)
|
NP_001094887.1:p.Glu346Ter
|
|
NM_001368197.1:c.1081G>T
(CRPPA)
|
NP_001355126.1:p.Glu361Ter
|
|
NR_160656.1:n.1251G>T
(CRPPA)
|
|
|