ENST00000229264.8:c.*263C>A
(GNB3)
MANE Select
|
ENSP00000229264.3:n.*263C>A
|
|
ENST00000229264.7:c.*263C>A
(GNB3)
|
ENSP00000229264.3:n.*263C>A
|
|
ENST00000422785.7:c.545-258G>T
(CDCA3)
|
ENSP00000415142.2:n.545-258G>T
|
|
ENST00000540458.5:n.2637C>A
(GNB3)
|
|
|
ENST00000542751.1:n.806C>A
(GNB3)
|
|
|
ENST00000603043.1:n.308-258G>T
(CDCA3)
|
|
|
ENST00000604599.1:n.813-258G>T
(CDCA3)
|
|
|
NM_001297571.1:c.*263C>A
(GNB3)
|
NP_001284500.1:n.*263C>A
|
|
NM_001297603.1:c.545-258G>T
(CDCA3)
|
NP_001284532.1:n.545-258G>T
|
|
NM_002075.3:c.*263C>A
(GNB3)
|
NP_002066.1:n.*263C>A
|
|
XM_011521027.1:c.*983-258G>T
(CDCA3)
|
XP_011519329.1:n.*983-258G>T
|
|
XM_011521028.1:c.*983-258G>T
(CDCA3)
|
XP_011519330.1:n.*983-258G>T
|
|
XM_011521029.1:c.*1201-258G>T
(CDCA3)
|
XP_011519331.1:n.*1201-258G>T
|
|
XM_011521030.1:c.*1134-258G>T
(CDCA3)
|
XP_011519332.1:n.*1134-258G>T
|
|
NM_001297603.2:c.545-258G>T
(CDCA3)
|
NP_001284532.1:n.545-258G>T
|
|
XR_001748879.2:n.2528-258G>T
(CDCA3)
|
|
|
XR_001748880.2:n.1879-258G>T
(CDCA3)
|
|
|
XR_001748881.2:n.1788-258G>T
(CDCA3)
|
|
|
XR_002957383.1:n.2030-258G>T
(CDCA3)
|
|
|
XR_002957384.1:n.2941-258G>T
(CDCA3)
|
|
|
XR_002957385.1:n.2421-258G>T
(CDCA3)
|
|
|
NM_001297571.2:c.*263C>A
(GNB3)
|
NP_001284500.1:n.*263C>A
|
|
NM_002075.4:c.*263C>A
(GNB3)
MANE Select
|
NP_002066.1:n.*263C>A
|
|
NM_001297603.3:c.545-258G>T
(CDCA3)
|
NP_001284532.1:n.545-258G>T
|
|