ENST00000378823.8:c.1836T>C
MANE Select
|
ENSP00000368100.4:p.Asn612=
|
|
ENST00000638452.2:c.1539T>C
|
ENSP00000492349.2:p.Asn513=
|
|
ENST00000638504.1:n.1480-193T>C
|
|
|
ENST00000638568.2:c.1539T>C
|
ENSP00000491158.2:p.Asn513=
|
|
ENST00000639899.1:n.2355T>C
|
|
|
ENST00000640655.2:c.1539T>C
|
ENSP00000491596.2:p.Asn513=
|
|
ENST00000651160.1:c.*16-193T>C
|
ENSP00000498829.1:n.*16-193T>C
|
|
ENST00000651658.1:n.2379T>C
|
|
|
ENST00000651723.1:c.*1919T>C
|
ENSP00000498237.1:n.*1919T>C
|
|
ENST00000652016.1:c.*89-193T>C
|
ENSP00000498267.1:n.*89-193T>C
|
|
ENST00000652485.1:c.1869T>C
|
ENSP00000498973.1:p.Asn623=
|
|
ENST00000378823.7:c.1836T>C
|
ENSP00000368100.4:p.Asn612=
|
|
ENST00000423956.5:c.*22T>C
|
ENSP00000390971.1:n.*22T>C
|
|
ENST00000453394.5:c.1653T>C
|
ENSP00000400049.1:p.Asn551=
|
|
ENST00000533482.5:c.*1462T>C
|
ENSP00000431225.1:n.*1462T>C
|
|
NM_005732.3:c.1836T>C
|
NP_005723.2:p.Asn612=
|
|
NM_005732.4:c.1836T>C
MANE Select
|
NP_005723.2:p.Asn612=
|
|