ENST00000229264.8:c.749G>T
(GNB3)
MANE Select
|
ENSP00000229264.3:p.Cys250Phe
|
|
ENST00000229264.7:c.749G>T
(GNB3)
|
ENSP00000229264.3:p.Cys250Phe
|
|
ENST00000422785.7:c.*1153C>A
(CDCA3)
|
ENSP00000415142.2:n.*1153C>A
|
|
ENST00000435982.6:c.746G>T
(GNB3)
|
ENSP00000414734.2:p.Cys249Phe
|
|
ENST00000537035.1:c.626G>T
(GNB3)
|
ENSP00000445967.1:p.Cys209Phe
|
|
ENST00000540458.5:n.2100G>T
(GNB3)
|
|
|
ENST00000542751.1:n.269G>T
(GNB3)
|
|
|
ENST00000603043.1:n.1219C>A
(CDCA3)
|
|
|
ENST00000604599.1:n.2081C>A
(CDCA3)
|
|
|
NM_001297571.1:c.746G>T
(GNB3)
|
NP_001284500.1:p.Cys249Phe
|
|
NM_002075.3:c.749G>T
(GNB3)
|
NP_002066.1:p.Cys250Phe
|
|
XM_011520953.1:c.749G>T
(GNB3)
|
XP_011519255.1:p.Cys250Phe
|
|
XM_011520954.1:c.746G>T
(GNB3)
|
XP_011519256.1:p.Cys249Phe
|
|
XM_011521027.1:c.*1894C>A
(CDCA3)
|
XP_011519329.1:n.*1894C>A
|
|
XM_011521028.1:c.*1894C>A
(CDCA3)
|
XP_011519330.1:n.*1894C>A
|
|
XM_011521029.1:c.*2112C>A
(CDCA3)
|
XP_011519331.1:n.*2112C>A
|
|
XM_011521030.1:c.*2045C>A
(CDCA3)
|
XP_011519332.1:n.*2045C>A
|
|
XM_011520953.3:c.749G>T
(GNB3)
|
XP_011519255.1:p.Cys250Phe
|
|
XR_001748879.2:n.3439C>A
(CDCA3)
|
|
|
XR_001748880.2:n.2790C>A
(CDCA3)
|
|
|
XR_001748881.2:n.2699C>A
(CDCA3)
|
|
|
XR_002957383.1:n.2941C>A
(CDCA3)
|
|
|
XR_002957384.1:n.3852C>A
(CDCA3)
|
|
|
XR_002957385.1:n.3332C>A
(CDCA3)
|
|
|
NM_001297571.2:c.746G>T
(GNB3)
|
NP_001284500.1:p.Cys249Phe
|
|
NM_002075.4:c.749G>T
(GNB3)
MANE Select
|
NP_002066.1:p.Cys250Phe
|
|
NM_001297603.3:c.*1153C>A
(CDCA3)
|
NP_001284532.1:n.*1153C>A
|
|