ENST00000378823.8:c.2602A>T
MANE Select
|
ENSP00000368100.4:p.Asn868Tyr
|
|
ENST00000638452.2:c.2305A>T
|
ENSP00000492349.2:p.Asn769Tyr
|
|
ENST00000638504.1:n.2210A>T
|
|
|
ENST00000638568.2:c.2305A>T
|
ENSP00000491158.2:p.Asn769Tyr
|
|
ENST00000639899.1:n.3121A>T
|
|
|
ENST00000640655.2:c.2305A>T
|
ENSP00000491596.2:p.Asn769Tyr
|
|
ENST00000651160.1:c.*746A>T
|
ENSP00000498829.1:n.*746A>T
|
|
ENST00000651723.1:c.*2685A>T
|
ENSP00000498237.1:n.*2685A>T
|
|
ENST00000652016.1:c.*819A>T
|
ENSP00000498267.1:n.*819A>T
|
|
ENST00000652485.1:c.2635A>T
|
ENSP00000498973.1:p.Asn879Tyr
|
|
ENST00000378823.7:c.2602A>T
|
ENSP00000368100.4:p.Asn868Tyr
|
|
ENST00000423956.5:c.*788A>T
|
ENSP00000390971.1:n.*788A>T
|
|
ENST00000533482.5:c.*2228A>T
|
ENSP00000431225.1:n.*2228A>T
|
|
NM_005732.3:c.2602A>T
|
NP_005723.2:p.Asn868Tyr
|
|
NM_005732.4:c.2602A>T
MANE Select
|
NP_005723.2:p.Asn868Tyr
|
|