ENST00000229264.8:c.728C>G
(GNB3)
MANE Select
|
ENSP00000229264.3:p.Thr243Arg
|
|
ENST00000229264.7:c.728C>G
(GNB3)
|
ENSP00000229264.3:p.Thr243Arg
|
|
ENST00000422785.7:c.*1174G>C
(CDCA3)
|
ENSP00000415142.2:n.*1174G>C
|
|
ENST00000435982.6:c.725C>G
(GNB3)
|
ENSP00000414734.2:p.Thr242Arg
|
|
ENST00000537035.1:c.605C>G
(GNB3)
|
ENSP00000445967.1:p.Thr202Arg
|
|
ENST00000540458.5:n.2079C>G
(GNB3)
|
|
|
ENST00000542751.1:n.248C>G
(GNB3)
|
|
|
ENST00000603043.1:n.1240G>C
(CDCA3)
|
|
|
ENST00000604599.1:n.2102G>C
(CDCA3)
|
|
|
NM_001297571.1:c.725C>G
(GNB3)
|
NP_001284500.1:p.Thr242Arg
|
|
NM_002075.3:c.728C>G
(GNB3)
|
NP_002066.1:p.Thr243Arg
|
|
XM_011520953.1:c.728C>G
(GNB3)
|
XP_011519255.1:p.Thr243Arg
|
|
XM_011520954.1:c.725C>G
(GNB3)
|
XP_011519256.1:p.Thr242Arg
|
|
XM_011521027.1:c.*1915G>C
(CDCA3)
|
XP_011519329.1:n.*1915G>C
|
|
XM_011521028.1:c.*1915G>C
(CDCA3)
|
XP_011519330.1:n.*1915G>C
|
|
XM_011521029.1:c.*2133G>C
(CDCA3)
|
XP_011519331.1:n.*2133G>C
|
|
XM_011521030.1:c.*2066G>C
(CDCA3)
|
XP_011519332.1:n.*2066G>C
|
|
XM_011520953.3:c.728C>G
(GNB3)
|
XP_011519255.1:p.Thr243Arg
|
|
XR_001748879.2:n.3460G>C
(CDCA3)
|
|
|
XR_001748880.2:n.2811G>C
(CDCA3)
|
|
|
XR_001748881.2:n.2720G>C
(CDCA3)
|
|
|
XR_002957383.1:n.2962G>C
(CDCA3)
|
|
|
XR_002957384.1:n.3873G>C
(CDCA3)
|
|
|
XR_002957385.1:n.3353G>C
(CDCA3)
|
|
|
NM_001297571.2:c.725C>G
(GNB3)
|
NP_001284500.1:p.Thr242Arg
|
|
NM_002075.4:c.728C>G
(GNB3)
MANE Select
|
NP_002066.1:p.Thr243Arg
|
|
NM_001297603.3:c.*1174G>C
(CDCA3)
|
NP_001284532.1:n.*1174G>C
|
|