ENST00000582970.6:c.12920C>G
(RNF213)
MANE Select
|
ENSP00000464087.1:p.Pro4307Arg
|
|
ENST00000411702.7:n.718C>G
(RNF213)
|
|
|
ENST00000508628.6:c.13067C>G
(RNF213)
|
ENSP00000425956.2:p.Pro4356Arg
|
|
ENST00000558116.5:n.2249C>G
(RNF213)
|
|
|
ENST00000573038.1:c.75C>G
(RNF213)
|
|
|
ENST00000582970.5:c.12920C>G
(RNF213)
|
ENSP00000464087.1:p.Pro4307Arg
|
|
NM_001256071.2:c.12920C>G
(RNF213)
|
NP_001243000.2:p.Pro4307Arg
|
|
NR_029376.1:n.241-17855G>C
(RNF213-AS1)
|
|
|
XM_005257545.3:c.13067C>G
(RNF213)
|
XP_005257602.2:p.Pro4356Arg
|
|
XM_005257546.3:c.13067C>G
(RNF213)
|
XP_005257603.2:p.Pro4356Arg
|
|
XM_006721995.2:c.13067C>G
(RNF213)
|
XP_006722058.1:p.Pro4356Arg
|
|
XM_011525084.1:c.13067C>G
(RNF213)
|
XP_011523386.1:p.Pro4356Arg
|
|
XM_011525085.1:c.13067C>G
(RNF213)
|
XP_011523387.1:p.Pro4356Arg
|
|
XR_243676.3:n.13238C>G
(RNF213)
|
|
|
XM_005257545.4:c.13067C>G
(RNF213)
|
XP_005257602.2:p.Pro4356Arg
|
|
XM_005257546.4:c.13067C>G
(RNF213)
|
XP_005257603.2:p.Pro4356Arg
|
|
XM_006721995.3:c.13067C>G
(RNF213)
|
XP_006722058.1:p.Pro4356Arg
|
|
XM_011525084.2:c.13067C>G
(RNF213)
|
XP_011523386.1:p.Pro4356Arg
|
|
XM_017024905.2:c.12062C>G
(RNF213)
|
XP_016880394.1:p.Pro4021Arg
|
|
NM_001256071.3:c.12920C>G
(RNF213)
MANE Select
|
NP_001243000.2:p.Pro4307Arg
|
|