ENST00000682114.1:c.413A>T
|
ENSP00000507245.1:p.Asp138Val
|
|
ENST00000682478.1:n.603A>T
|
|
|
ENST00000683576.1:n.603A>T
|
|
|
ENST00000683627.1:c.413A>T
|
ENSP00000507533.1:p.Asp138Val
|
|
ENST00000684082.1:c.370A>T
|
ENSP00000508266.1:n.370A>T
|
|
ENST00000684633.1:n.385A>T
|
|
|
ENST00000684678.1:c.409A>T
|
ENSP00000507059.1:n.409A>T
|
|
ENST00000369842.9:c.413A>T
MANE Select
|
ENSP00000358857.4:p.Asp138Val
|
|
ENST00000369835.3:c.308A>T
|
ENSP00000358850.3:p.Asp103Val
|
|
ENST00000369842.8:c.413A>T
|
ENSP00000358857.4:p.Asp138Val
|
|
ENST00000428228.5:c.*318A>T
|
ENSP00000401081.1:n.*318A>T
|
|
ENST00000468294.5:n.373A>T
|
|
|
ENST00000471965.1:n.202A>T
|
|
|
ENST00000485261.1:n.603A>T
|
|
|
ENST00000486738.5:n.771A>T
|
|
|
ENST00000492448.1:n.396A>T
|
|
|
NM_000117.2:c.413A>T , LRG_745t1:c.413A>T
|
NP_000108.1:p.Asp138Val
|
|
XM_024452349.1:c.419A>T
|
XP_024308117.1:p.Asp140Val
|
|
NM_000117.3:c.413A>T
MANE Select
|
NP_000108.1:p.Asp138Val
|
|