ENST00000267750.9:c.357T>G
MANE Select
|
ENSP00000267750.4:p.Thr119=
|
|
ENST00000249209.8:c.355+584T>G
|
ENSP00000249209.4:n.355+584T>G
|
|
ENST00000267750.8:c.357T>G
|
ENSP00000267750.4:p.Thr119=
|
|
ENST00000557879.1:c.*302T>G
|
ENSP00000473881.1:n.*302T>G
|
|
ENST00000558102.1:c.*108+584T>G
|
ENSP00000453880.1:n.*108+584T>G
|
|
ENST00000558205.5:c.*110T>G
|
ENSP00000454042.1:n.*110T>G
|
|
ENST00000559078.5:c.304-536T>G
|
ENSP00000454052.1:n.304-536T>G
|
|
ENST00000559421.1:c.202-1323T>G
|
ENSP00000452672.1:n.202-1323T>G
|
|
ENST00000560911.5:c.*110T>G
|
ENSP00000453610.1:n.*110T>G
|
|
ENST00000560947.1:c.153-7T>G
|
|
|
ENST00000561246.1:n.1313+606T>G
|
|
|
NM_001286420.1:c.355+584T>G
|
NP_001273349.1:n.355+584T>G
|
|
NM_016454.3:c.357T>G
|
NP_057538.1:p.Thr119=
|
|
NM_001351373.1:c.114T>G
|
NP_001338302.1:p.Thr38=
|
|
NR_147140.1:n.481+584T>G
|
|
|
NM_016454.4:c.357T>G
MANE Select
|
NP_057538.1:p.Thr119=
|
|
NM_001286420.2:c.355+584T>G
|
NP_001273349.1:n.355+584T>G
|
|
NM_001351373.2:c.114T>G
|
NP_001338302.1:p.Thr38=
|
|
NR_147140.2:n.462+584T>G
|
|
|