|
ENST00000539493.3:c.2914+1333G>T
(RAB3GAP1)
|
ENSP00000444306.2:n.2914+1333G>T
|
|
|
ENST00000685652.1:n.4886G>T
(RAB3GAP1)
|
|
|
|
ENST00000685967.1:c.*3704G>T
(RAB3GAP1)
|
ENSP00000508423.1:n.*3704G>T
|
|
|
ENST00000687199.1:c.*4336G>T
(RAB3GAP1)
|
ENSP00000510319.1:n.*4336G>T
|
|
|
ENST00000688088.1:n.7429G>T
(RAB3GAP1)
|
|
|
|
ENST00000690208.1:c.*3925G>T
(RAB3GAP1)
|
ENSP00000510746.1:n.*3925G>T
|
|
|
ENST00000691339.1:c.*3891G>T
(RAB3GAP1)
|
ENSP00000509953.1:n.*3891G>T
|
|
|
ENST00000691478.1:c.*4346G>T
(RAB3GAP1)
|
ENSP00000509081.1:n.*4346G>T
|
|
|
ENST00000692993.1:n.1826G>T
(RAB3GAP1)
|
|
|
|
ENST00000693554.1:c.*2070G>T
(RAB3GAP1)
|
ENSP00000509030.1:n.*2070G>T
|
|
|
ENST00000264158.13:c.*1301G>T
(RAB3GAP1)
MANE Select
|
ENSP00000264158.8:n.*1301G>T
|
|
|
ENST00000264158.12:c.*1301G>T
(RAB3GAP1)
|
ENSP00000264158.7:n.*1301G>T
|
|
|
ENST00000412849.5:n.1782-4928C>A
(ZRANB3)
|
|
|
|
ENST00000487003.5:n.3098+234G>T
(RAB3GAP1)
|
|
|
|
ENST00000539493.2:c.2897+234G>T
(RAB3GAP1)
|
ENSP00000444306.1:n.2897+234G>T
|
|
|
ENST00000619650.4:c.1618-4928C>A
(ZRANB3)
|
ENSP00000480120.1:n.1618-4928C>A
|
|
|
NM_001172435.1:c.*1301G>T
(RAB3GAP1)
|
NP_001165906.1:n.*1301G>T
|
|
|
NM_012233.2:c.*1301G>T
(RAB3GAP1)
|
NP_036365.1:n.*1301G>T
|
|
|
XM_011510822.1:c.2935+1333G>T
(RAB3GAP1)
|
XP_011509124.1:n.2935+1333G>T
|
|
|
XM_011510823.1:c.2914+1333G>T
(RAB3GAP1)
|
XP_011509125.1:n.2914+1333G>T
|
|
|
XM_011510824.1:c.*323G>T
(RAB3GAP1)
|
XP_011509126.1:n.*323G>T
|
|
|
XM_011510825.1:c.*323G>T
(RAB3GAP1)
|
XP_011509127.1:n.*323G>T
|
|
|
XM_011510823.3:c.2914+1333G>T
(RAB3GAP1)
|
XP_011509125.1:n.2914+1333G>T
|
|
|
XM_011510825.3:c.*323G>T
(RAB3GAP1)
|
XP_011509127.1:n.*323G>T
|
|
|
XM_011511966.3:c.3049-4928C>A
(ZRANB3)
|
XP_011510268.2:n.3049-4928C>A
|
|
|
XR_001738674.2:n.2941+1333G>T
(RAB3GAP1)
|
|
|
|
NM_001172435.2:c.*1301G>T
(RAB3GAP1)
|
NP_001165906.1:n.*1301G>T
|
|
|
NM_012233.3:c.*1301G>T
(RAB3GAP1)
MANE Select
|
NP_036365.1:n.*1301G>T
|
|
