|
ENST00000636581.2:n.3850A>T
(CACNA1D)
|
|
|
|
ENST00000636633.2:n.5460A>T
(CACNA1D)
|
|
|
|
ENST00000636999.2:n.3896A>T
(CACNA1D)
|
|
|
|
ENST00000288139.11:c.*1975A>T
(CACNA1D)
MANE Plus Clinical
|
ENSP00000288139.3:n.*1975A>T
|
|
|
ENST00000315251.11:c.*4396T>A
(CHDH)
MANE Select
|
ENSP00000319851.5:n.*4396T>A
|
|
|
ENST00000350061.11:c.*1975A>T
(CACNA1D)
MANE Select
|
ENSP00000288133.5:n.*1975A>T
|
|
|
ENST00000636999.1:n.3888A>T
(CACNA1D)
|
|
|
|
ENST00000288139.8:c.*1975A>T
(CACNA1D)
|
ENSP00000288139.3:n.*1975A>T
|
|
|
ENST00000315251.10:c.*4396T>A
(CHDH)
|
ENSP00000319851.5:n.*4396T>A
|
|
|
XM_006713250.4:c.*4396T>A
(CHDH)
|
XP_006713313.1:n.*4396T>A
|
|
|
XM_006713251.4:c.*4396T>A
(CHDH)
|
XP_006713314.1:n.*4396T>A
|
|
|
XM_006713252.4:c.*4808T>A
(CHDH)
|
XP_006713315.1:n.*4808T>A
|
|
|
XM_011533938.3:c.*4396T>A
(CHDH)
|
XP_011532240.1:n.*4396T>A
|
|
|
XM_011533939.3:c.*4396T>A
(CHDH)
|
XP_011532241.1:n.*4396T>A
|
|
|
XM_017006797.2:c.*4396T>A
(CHDH)
|
XP_016862286.1:n.*4396T>A
|
|
|
XM_017006798.2:c.*4396T>A
(CHDH)
|
XP_016862287.1:n.*4396T>A
|
|
|
XM_017006799.2:c.*4808T>A
(CHDH)
|
XP_016862288.1:n.*4808T>A
|
|
|
XR_002959545.1:n.4351-326T>A
(CHDH)
|
|
|
|
NM_001128840.3:c.*1975A>T
(CACNA1D)
MANE Select
|
NP_001122312.1:n.*1975A>T
|
|
|
NM_018397.5:c.*4396T>A
(CHDH)
MANE Select
|
NP_060867.2:n.*4396T>A
|
|
|
NM_000720.4:c.*1975A>T
(CACNA1D)
MANE Plus Clinical
|
NP_000711.1:n.*1975A>T
|
|
|
NM_001128839.3:c.*1975A>T
(CACNA1D)
|
NP_001122311.1:n.*1975A>T
|
|
