ENST00000229264.8:c.832T>C
(GNB3)
MANE Select
|
ENSP00000229264.3:p.Phe278Leu
|
|
ENST00000229264.7:c.832T>C
(GNB3)
|
ENSP00000229264.3:p.Phe278Leu
|
|
ENST00000422785.7:c.*1070A>G
(CDCA3)
|
ENSP00000415142.2:n.*1070A>G
|
|
ENST00000435982.6:c.829T>C
(GNB3)
|
ENSP00000414734.2:p.Phe277Leu
|
|
ENST00000537035.1:c.709T>C
(GNB3)
|
ENSP00000445967.1:p.Phe237Leu
|
|
ENST00000540458.5:n.2183T>C
(GNB3)
|
|
|
ENST00000542751.1:n.352T>C
(GNB3)
|
|
|
ENST00000603043.1:n.1136A>G
(CDCA3)
|
|
|
ENST00000604599.1:n.1998A>G
(CDCA3)
|
|
|
NM_001297571.1:c.829T>C
(GNB3)
|
NP_001284500.1:p.Phe277Leu
|
|
NM_002075.3:c.832T>C
(GNB3)
|
NP_002066.1:p.Phe278Leu
|
|
XM_011520953.1:c.832T>C
(GNB3)
|
XP_011519255.1:p.Phe278Leu
|
|
XM_011520954.1:c.829T>C
(GNB3)
|
XP_011519256.1:p.Phe277Leu
|
|
XM_011521027.1:c.*1811A>G
(CDCA3)
|
XP_011519329.1:n.*1811A>G
|
|
XM_011521028.1:c.*1811A>G
(CDCA3)
|
XP_011519330.1:n.*1811A>G
|
|
XM_011521029.1:c.*2029A>G
(CDCA3)
|
XP_011519331.1:n.*2029A>G
|
|
XM_011521030.1:c.*1962A>G
(CDCA3)
|
XP_011519332.1:n.*1962A>G
|
|
XM_011520953.3:c.832T>C
(GNB3)
|
XP_011519255.1:p.Phe278Leu
|
|
XR_001748879.2:n.3356A>G
(CDCA3)
|
|
|
XR_001748880.2:n.2707A>G
(CDCA3)
|
|
|
XR_001748881.2:n.2616A>G
(CDCA3)
|
|
|
XR_002957383.1:n.2858A>G
(CDCA3)
|
|
|
XR_002957384.1:n.3769A>G
(CDCA3)
|
|
|
XR_002957385.1:n.3249A>G
(CDCA3)
|
|
|
NM_001297571.2:c.829T>C
(GNB3)
|
NP_001284500.1:p.Phe277Leu
|
|
NM_002075.4:c.832T>C
(GNB3)
MANE Select
|
NP_002066.1:p.Phe278Leu
|
|
NM_001297603.3:c.*1070A>G
(CDCA3)
|
NP_001284532.1:n.*1070A>G
|
|