|
ENST00000503594.6:c.545C>T
(CTBP1)
|
ENSP00000422148.2:p.Ala182Val
|
|
|
ENST00000703138.1:c.545C>T
(CTBP1)
|
ENSP00000515195.1:p.Ala182Val
|
|
|
ENST00000703163.1:c.545C>T
(CTBP1)
|
ENSP00000515211.1:p.Ala182Val
|
|
|
ENST00000703164.1:c.545C>T
(CTBP1)
|
ENSP00000515212.1:p.Ala182Val
|
|
|
ENST00000703165.1:c.545C>T
(CTBP1)
|
ENSP00000515213.1:p.Ala182Val
|
|
|
ENST00000382952.8:c.545C>T
(CTBP1)
MANE Select
|
ENSP00000372411.3:p.Ala182Val
|
|
|
ENST00000290921.10:c.578C>T
(CTBP1)
|
ENSP00000290921.6:p.Ala193Val
|
|
|
ENST00000382952.7:c.545C>T
(CTBP1)
|
ENSP00000372411.3:p.Ala182Val
|
|
|
ENST00000504092.5:c.117C>T
(CTBP1)
|
|
|
|
ENST00000505826.5:n.420C>T
(CTBP1)
|
|
|
|
ENST00000506180.5:c.560C>T
(CTBP1)
|
|
|
|
ENST00000510739.1:c.61C>T
(CTBP1)
|
|
|
|
ENST00000511907.1:n.233C>T
(CTBP1)
|
|
|
|
ENST00000514669.5:n.720C>T
(CTBP1)
|
|
|
|
NM_001012614.1:c.545C>T
(CTBP1)
|
NP_001012632.1:p.Ala182Val
|
|
|
NM_001328.2:c.578C>T
(CTBP1)
|
NP_001319.1:p.Ala193Val
|
|
|
NR_104331.1:n.1470G>A
(CTBP1-AS)
|
|
|
|
XM_005272261.2:c.578C>T
(CTBP1)
|
XP_005272318.1:p.Ala193Val
|
|
|
XM_005272263.3:c.545C>T
(CTBP1)
|
XP_005272320.1:p.Ala182Val
|
|
|
XM_011513395.1:c.545C>T
(CTBP1)
|
XP_011511697.1:p.Ala182Val
|
|
|
XM_011513396.1:c.545C>T
(CTBP1)
|
XP_011511698.1:p.Ala182Val
|
|
|
XM_011513397.1:c.356C>T
(CTBP1)
|
XP_011511699.1:p.Ala119Val
|
|
|
XM_005272261.3:c.578C>T
(CTBP1)
|
XP_005272318.1:p.Ala193Val
|
|
|
XM_005272263.5:c.545C>T
(CTBP1)
|
XP_005272320.1:p.Ala182Val
|
|
|
XM_011513395.3:c.545C>T
(CTBP1)
|
XP_011511697.1:p.Ala182Val
|
|
|
XM_011513396.3:c.545C>T
(CTBP1)
|
XP_011511698.1:p.Ala182Val
|
|
|
XM_017007762.2:c.545C>T
(CTBP1)
|
XP_016863251.1:p.Ala182Val
|
|
|
XM_017007763.2:c.545C>T
(CTBP1)
|
XP_016863252.1:p.Ala182Val
|
|
|
XM_017007764.1:c.545C>T
(CTBP1)
|
XP_016863253.1:p.Ala182Val
|
|
|
XM_017007765.2:c.545C>T
(CTBP1)
|
XP_016863254.1:p.Ala182Val
|
|
|
XM_017007766.2:c.545C>T
(CTBP1)
|
XP_016863255.1:p.Ala182Val
|
|
|
XM_017007767.2:c.545C>T
(CTBP1)
|
XP_016863256.1:p.Ala182Val
|
|
|
XM_024453899.1:c.356C>T
(CTBP1)
|
XP_024309667.1:p.Ala119Val
|
|
|
NM_001012614.2:c.545C>T
(CTBP1)
MANE Select
|
NP_001012632.1:p.Ala182Val
|
|
|
NM_001328.3:c.578C>T
(CTBP1)
|
NP_001319.1:p.Ala193Val
|
|
|
NM_001377186.1:c.578C>T
(CTBP1)
|
NP_001364115.1:p.Ala193Val
|
|
|
NM_001377187.1:c.545C>T
(CTBP1)
|
NP_001364116.1:p.Ala182Val
|
|
|
NM_001377188.1:c.545C>T
(CTBP1)
|
NP_001364117.1:p.Ala182Val
|
|
|
NM_001377189.1:c.545C>T
(CTBP1)
|
NP_001364118.1:p.Ala182Val
|
|
|
NM_001377190.1:c.545C>T
(CTBP1)
|
NP_001364119.1:p.Ala182Val
|
|
|
NM_001377191.1:c.545C>T
(CTBP1)
|
NP_001364120.1:p.Ala182Val
|
|
|
NM_001377192.1:c.545C>T
(CTBP1)
|
NP_001364121.1:p.Ala182Val
|
|
|
NM_001377193.1:c.545C>T
(CTBP1)
|
NP_001364122.1:p.Ala182Val
|
|
