ENST00000229264.8:c.732C>T
(GNB3)
MANE Select
|
ENSP00000229264.3:p.Gly244=
|
|
ENST00000229264.7:c.732C>T
(GNB3)
|
ENSP00000229264.3:p.Gly244=
|
|
ENST00000422785.7:c.*1170G>A
(CDCA3)
|
ENSP00000415142.2:n.*1170G>A
|
|
ENST00000435982.6:c.729C>T
(GNB3)
|
ENSP00000414734.2:p.Gly243=
|
|
ENST00000537035.1:c.609C>T
(GNB3)
|
ENSP00000445967.1:p.Gly203=
|
|
ENST00000540458.5:n.2083C>T
(GNB3)
|
|
|
ENST00000542751.1:n.252C>T
(GNB3)
|
|
|
ENST00000603043.1:n.1236G>A
(CDCA3)
|
|
|
ENST00000604599.1:n.2098G>A
(CDCA3)
|
|
|
NM_001297571.1:c.729C>T
(GNB3)
|
NP_001284500.1:p.Gly243=
|
|
NM_002075.3:c.732C>T
(GNB3)
|
NP_002066.1:p.Gly244=
|
|
XM_011520953.1:c.732C>T
(GNB3)
|
XP_011519255.1:p.Gly244=
|
|
XM_011520954.1:c.729C>T
(GNB3)
|
XP_011519256.1:p.Gly243=
|
|
XM_011521027.1:c.*1911G>A
(CDCA3)
|
XP_011519329.1:n.*1911G>A
|
|
XM_011521028.1:c.*1911G>A
(CDCA3)
|
XP_011519330.1:n.*1911G>A
|
|
XM_011521029.1:c.*2129G>A
(CDCA3)
|
XP_011519331.1:n.*2129G>A
|
|
XM_011521030.1:c.*2062G>A
(CDCA3)
|
XP_011519332.1:n.*2062G>A
|
|
XM_011520953.3:c.732C>T
(GNB3)
|
XP_011519255.1:p.Gly244=
|
|
XR_001748879.2:n.3456G>A
(CDCA3)
|
|
|
XR_001748880.2:n.2807G>A
(CDCA3)
|
|
|
XR_001748881.2:n.2716G>A
(CDCA3)
|
|
|
XR_002957383.1:n.2958G>A
(CDCA3)
|
|
|
XR_002957384.1:n.3869G>A
(CDCA3)
|
|
|
XR_002957385.1:n.3349G>A
(CDCA3)
|
|
|
NM_001297571.2:c.729C>T
(GNB3)
|
NP_001284500.1:p.Gly243=
|
|
NM_002075.4:c.732C>T
(GNB3)
MANE Select
|
NP_002066.1:p.Gly244=
|
|
NM_001297603.3:c.*1170G>A
(CDCA3)
|
NP_001284532.1:n.*1170G>A
|
|