ENST00000257904.11:c.821A>G
(CDK4)
MANE Select
|
ENSP00000257904.5:p.Glu274Gly
|
|
ENST00000257910.8:c.*1326T>C
(TSPAN31)
MANE Select
|
ENSP00000257910.3:n.*1326T>C
|
|
ENST00000257904.10:c.821A>G
(CDK4)
|
ENSP00000257904.5:p.Glu274Gly
|
|
ENST00000312990.10:c.*133A>G
(CDK4)
|
ENSP00000316889.6:n.*133A>G
|
|
ENST00000546489.5:c.599A>G
(CDK4)
|
ENSP00000447779.1:p.Glu200Gly
|
|
ENST00000547992.5:c.*1326T>C
(TSPAN31)
|
ENSP00000448209.1:n.*1326T>C
|
|
ENST00000549606.5:c.32A>G
(CDK4)
|
ENSP00000447005.1:p.Glu11Gly
|
|
ENST00000552713.5:n.480A>G
(CDK4)
|
|
|
ENST00000553237.5:c.*460A>G
(CDK4)
|
ENSP00000448885.1:n.*460A>G
|
|
NM_000075.3:c.821A>G
(CDK4)
|
NP_000066.1:p.Glu274Gly
|
|
NM_000075.4:c.821A>G
(CDK4)
MANE Select
|
NP_000066.1:p.Glu274Gly
|
|
NM_005981.5:c.*1326T>C
(TSPAN31)
MANE Select
|
NP_005972.1:n.*1326T>C
|
|
NM_001330168.2:c.*1326T>C
(TSPAN31)
|
NP_001317097.1:n.*1326T>C
|
|
NM_001330169.2:c.*1326T>C
(TSPAN31)
|
NP_001317098.1:n.*1326T>C
|
|