ENST00000378823.8:c.1858G=
MANE Select
|
ENSP00000368100.4:p.Glu620=
|
|
ENST00000638452.2:c.1561G=
|
ENSP00000492349.2:p.Glu521=
|
|
ENST00000638504.1:n.1480-171G=
|
|
|
ENST00000638568.2:c.1561G=
|
ENSP00000491158.2:p.Glu521=
|
|
ENST00000639899.1:n.2377G=
|
|
|
ENST00000640655.2:c.1561G=
|
ENSP00000491596.2:p.Glu521=
|
|
ENST00000651160.1:c.*16-171G=
|
ENSP00000498829.1:n.*16-171G=
|
|
ENST00000651658.1:n.2401G=
|
|
|
ENST00000651723.1:c.*1941G=
|
ENSP00000498237.1:n.*1941G=
|
|
ENST00000652016.1:c.*89-171G=
|
ENSP00000498267.1:n.*89-171G=
|
|
ENST00000652485.1:c.1891G=
|
ENSP00000498973.1:p.Glu631=
|
|
ENST00000378823.7:c.1858G=
|
ENSP00000368100.4:p.Glu620=
|
|
ENST00000423956.5:c.*44G=
|
ENSP00000390971.1:n.*44G=
|
|
ENST00000453394.5:c.1675G=
|
ENSP00000400049.1:p.Glu559=
|
|
ENST00000533482.5:c.*1484G=
|
ENSP00000431225.1:n.*1484G=
|
|
NM_005732.3:c.1858G=
|
NP_005723.2:p.Glu620=
|
|
NM_005732.4:c.1858G=
MANE Select
|
NP_005723.2:p.Glu620=
|
|