ENST00000582970.6:c.12875T>C
(RNF213)
MANE Select
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ENSP00000464087.1:p.Val4292Ala
|
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ENST00000411702.7:n.673T>C
(RNF213)
|
|
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ENST00000508628.6:c.13022T>C
(RNF213)
|
ENSP00000425956.2:p.Val4341Ala
|
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ENST00000558116.5:n.2204T>C
(RNF213)
|
|
|
ENST00000573038.1:c.30T>C
(RNF213)
|
|
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ENST00000582970.5:c.12875T>C
(RNF213)
|
ENSP00000464087.1:p.Val4292Ala
|
|
NM_001256071.2:c.12875T>C
(RNF213)
|
NP_001243000.2:p.Val4292Ala
|
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NR_029376.1:n.241-17810A>G
(RNF213-AS1)
|
|
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XM_005257545.3:c.13022T>C
(RNF213)
|
XP_005257602.2:p.Val4341Ala
|
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XM_005257546.3:c.13022T>C
(RNF213)
|
XP_005257603.2:p.Val4341Ala
|
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XM_006721995.2:c.13022T>C
(RNF213)
|
XP_006722058.1:p.Val4341Ala
|
|
XM_011525084.1:c.13022T>C
(RNF213)
|
XP_011523386.1:p.Val4341Ala
|
|
XM_011525085.1:c.13022T>C
(RNF213)
|
XP_011523387.1:p.Val4341Ala
|
|
XR_243676.3:n.13193T>C
(RNF213)
|
|
|
XM_005257545.4:c.13022T>C
(RNF213)
|
XP_005257602.2:p.Val4341Ala
|
|
XM_005257546.4:c.13022T>C
(RNF213)
|
XP_005257603.2:p.Val4341Ala
|
|
XM_006721995.3:c.13022T>C
(RNF213)
|
XP_006722058.1:p.Val4341Ala
|
|
XM_011525084.2:c.13022T>C
(RNF213)
|
XP_011523386.1:p.Val4341Ala
|
|
XM_017024905.2:c.12017T>C
(RNF213)
|
XP_016880394.1:p.Val4006Ala
|
|
NM_001256071.3:c.12875T>C
(RNF213)
MANE Select
|
NP_001243000.2:p.Val4292Ala
|
|