ENST00000378823.8:c.2603A>T
MANE Select
|
ENSP00000368100.4:p.Asn868Ile
|
|
ENST00000638452.2:c.2306A>T
|
ENSP00000492349.2:p.Asn769Ile
|
|
ENST00000638504.1:n.2211A>T
|
|
|
ENST00000638568.2:c.2306A>T
|
ENSP00000491158.2:p.Asn769Ile
|
|
ENST00000639899.1:n.3122A>T
|
|
|
ENST00000640655.2:c.2306A>T
|
ENSP00000491596.2:p.Asn769Ile
|
|
ENST00000651160.1:c.*747A>T
|
ENSP00000498829.1:n.*747A>T
|
|
ENST00000651723.1:c.*2686A>T
|
ENSP00000498237.1:n.*2686A>T
|
|
ENST00000652016.1:c.*820A>T
|
ENSP00000498267.1:n.*820A>T
|
|
ENST00000652485.1:c.2636A>T
|
ENSP00000498973.1:p.Asn879Ile
|
|
ENST00000378823.7:c.2603A>T
|
ENSP00000368100.4:p.Asn868Ile
|
|
ENST00000423956.5:c.*789A>T
|
ENSP00000390971.1:n.*789A>T
|
|
ENST00000533482.5:c.*2229A>T
|
ENSP00000431225.1:n.*2229A>T
|
|
NM_005732.3:c.2603A>T
|
NP_005723.2:p.Asn868Ile
|
|
NM_005732.4:c.2603A>T
MANE Select
|
NP_005723.2:p.Asn868Ile
|
|