ENST00000257904.11:c.850A>G
(CDK4)
MANE Select
|
ENSP00000257904.5:p.Ile284Val
|
|
ENST00000257910.8:c.*1297T>C
(TSPAN31)
MANE Select
|
ENSP00000257910.3:n.*1297T>C
|
|
ENST00000257904.10:c.850A>G
(CDK4)
|
ENSP00000257904.5:p.Ile284Val
|
|
ENST00000312990.10:c.*162A>G
(CDK4)
|
ENSP00000316889.6:n.*162A>G
|
|
ENST00000547992.5:c.*1297T>C
(TSPAN31)
|
ENSP00000448209.1:n.*1297T>C
|
|
ENST00000549606.5:c.61A>G
(CDK4)
|
ENSP00000447005.1:p.Ile21Val
|
|
ENST00000552713.5:n.509A>G
(CDK4)
|
|
|
ENST00000553237.5:c.*489A>G
(CDK4)
|
ENSP00000448885.1:n.*489A>G
|
|
NM_000075.3:c.850A>G
(CDK4)
|
NP_000066.1:p.Ile284Val
|
|
NM_000075.4:c.850A>G
(CDK4)
MANE Select
|
NP_000066.1:p.Ile284Val
|
|
NM_005981.5:c.*1297T>C
(TSPAN31)
MANE Select
|
NP_005972.1:n.*1297T>C
|
|
NM_001330168.2:c.*1297T>C
(TSPAN31)
|
NP_001317097.1:n.*1297T>C
|
|
NM_001330169.2:c.*1297T>C
(TSPAN31)
|
NP_001317098.1:n.*1297T>C
|
|