ENST00000582970.6:c.12753G>C
(RNF213)
MANE Select
|
ENSP00000464087.1:p.Glu4251Asp
|
|
ENST00000411702.7:n.551G>C
(RNF213)
|
|
|
ENST00000508628.6:c.12900G>C
(RNF213)
|
ENSP00000425956.2:p.Glu4300Asp
|
|
ENST00000558116.5:n.2082G>C
(RNF213)
|
|
|
ENST00000582970.5:c.12753G>C
(RNF213)
|
ENSP00000464087.1:p.Glu4251Asp
|
|
NM_001256071.2:c.12753G>C
(RNF213)
|
NP_001243000.2:p.Glu4251Asp
|
|
NR_029376.1:n.241-17688C>G
(RNF213-AS1)
|
|
|
XM_005257545.3:c.12900G>C
(RNF213)
|
XP_005257602.2:p.Glu4300Asp
|
|
XM_005257546.3:c.12900G>C
(RNF213)
|
XP_005257603.2:p.Glu4300Asp
|
|
XM_006721995.2:c.12900G>C
(RNF213)
|
XP_006722058.1:p.Glu4300Asp
|
|
XM_011525084.1:c.12900G>C
(RNF213)
|
XP_011523386.1:p.Glu4300Asp
|
|
XM_011525085.1:c.12900G>C
(RNF213)
|
XP_011523387.1:p.Glu4300Asp
|
|
XR_243676.3:n.13071G>C
(RNF213)
|
|
|
XM_005257545.4:c.12900G>C
(RNF213)
|
XP_005257602.2:p.Glu4300Asp
|
|
XM_005257546.4:c.12900G>C
(RNF213)
|
XP_005257603.2:p.Glu4300Asp
|
|
XM_006721995.3:c.12900G>C
(RNF213)
|
XP_006722058.1:p.Glu4300Asp
|
|
XM_011525084.2:c.12900G>C
(RNF213)
|
XP_011523386.1:p.Glu4300Asp
|
|
XM_017024905.2:c.11895G>C
(RNF213)
|
XP_016880394.1:p.Glu3965Asp
|
|
NM_001256071.3:c.12753G>C
(RNF213)
MANE Select
|
NP_001243000.2:p.Glu4251Asp
|
|