ENST00000242152.7:c.289T>A
MANE Select
|
ENSP00000242152.2:p.Trp97Arg
|
|
ENST00000242152.6:c.289T>A
|
ENSP00000242152.2:p.Trp97Arg
|
|
ENST00000405982.1:c.289T>A
|
ENSP00000385282.1:p.Trp97Arg
|
|
ENST00000407573.5:c.289T>A
|
ENSP00000384364.1:p.Trp97Arg
|
|
NM_000905.3:c.289T>A
|
NP_000896.1:p.Trp97Arg
|
|
XM_017012910.1:c.41+27675A>T
|
XP_016868399.1:n.41+27675A>T
|
|
XM_017012911.1:c.41+27675A>T
|
XP_016868400.1:n.41+27675A>T
|
|
XR_001745121.1:n.473+27675A>T
|
|
|
XR_001745122.1:n.345-94653A>T
|
|
|
XR_001745123.1:n.473+27675A>T
|
|
|
XR_001745124.1:n.473+27675A>T
|
|
|
XR_001745125.1:n.473+27675A>T
|
|
|
XR_001745126.1:n.473+27675A>T
|
|
|
XR_001745127.1:n.345-35983A>T
|
|
|
XR_001745129.1:n.473+27675A>T
|
|
|
XR_001745130.1:n.473+27675A>T
|
|
|
XR_001745131.1:n.473+27675A>T
|
|
|
XR_001745132.1:n.473+27675A>T
|
|
|
NM_000905.4:c.289T>A
MANE Select
|
NP_000896.1:p.Trp97Arg
|
|