ENST00000339157.10:c.824T>A
MANE Select
|
ENSP00000341408.5:p.Phe275Tyr
|
|
ENST00000376542.8:c.824T>A
|
ENSP00000365725.3:p.Phe275Tyr
|
|
ENST00000465694.2:c.278T>A
|
ENSP00000459278.2:p.Phe93Tyr
|
|
ENST00000671784.1:c.278T>A
|
ENSP00000500451.1:p.Phe93Tyr
|
|
ENST00000671858.1:c.278T>A
|
ENSP00000500550.1:p.Phe93Tyr
|
|
ENST00000672001.1:n.335T>A
|
|
|
ENST00000672114.1:c.278T>A
|
ENSP00000499945.1:p.Phe93Tyr
|
|
ENST00000672258.1:c.278T>A
|
ENSP00000499868.1:p.Phe93Tyr
|
|
ENST00000672331.1:c.278T>A
|
ENSP00000500286.1:p.Phe93Tyr
|
|
ENST00000672358.1:c.278T>A
|
ENSP00000500062.1:p.Phe93Tyr
|
|
ENST00000672406.1:c.*163T>A
|
ENSP00000500208.1:n.*163T>A
|
|
ENST00000672566.1:c.353T>A
|
ENSP00000500106.1:p.Phe118Tyr
|
|
ENST00000672596.1:c.278T>A
|
ENSP00000500290.1:p.Phe93Tyr
|
|
ENST00000672871.1:c.278T>A
|
ENSP00000499949.1:p.Phe93Tyr
|
|
ENST00000673094.1:c.278T>A
|
ENSP00000500257.1:p.Phe93Tyr
|
|
ENST00000673121.1:c.380T>A
|
ENSP00000499839.1:p.Phe127Tyr
|
|
ENST00000673227.1:c.278T>A
|
ENSP00000500514.1:p.Phe93Tyr
|
|
ENST00000673524.1:c.386T>A
|
|
|
ENST00000339157.9:c.824T>A
|
ENSP00000341408.5:p.Phe275Tyr
|
|
ENST00000376542.7:c.824T>A
|
ENSP00000365725.3:p.Phe275Tyr
|
|
ENST00000481556.1:n.478T>A
|
|
|
ENST00000491682.5:c.353T>A
|
ENSP00000459495.1:p.Phe118Tyr
|
|
ENST00000576316.5:c.128T>A
|
ENSP00000459121.1:p.Phe43Tyr
|
|
NM_001042472.2:c.824T>A
|
NP_001035937.1:p.Phe275Tyr
|
|
NM_015600.4:c.824T>A
|
NP_056415.1:p.Phe275Tyr
|
|
XM_005260698.1:c.824T>A
|
XP_005260755.1:p.Phe275Tyr
|
|
XM_005260699.3:c.824T>A
|
XP_005260756.1:p.Phe275Tyr
|
|
XM_005260700.1:c.353T>A
|
XP_005260757.1:p.Phe118Tyr
|
|
XM_011529214.1:c.824T>A
|
XP_011527516.1:p.Phe275Tyr
|
|
XM_011529215.1:c.353T>A
|
XP_011527517.1:p.Phe118Tyr
|
|
XM_011529216.1:c.353T>A
|
XP_011527518.1:p.Phe118Tyr
|
|
XM_011529217.1:c.167T>A
|
XP_011527519.1:p.Phe56Tyr
|
|
XM_011529218.1:c.167T>A
|
XP_011527520.1:p.Phe56Tyr
|
|
XM_011529214.2:c.824T>A
|
XP_011527516.1:p.Phe275Tyr
|
|
XM_017027796.1:c.353T>A
|
XP_016883285.1:p.Phe118Tyr
|
|
XR_002958465.1:n.834T>A
|
|
|
XR_002958466.1:n.954T>A
|
|
|
XR_002958467.1:n.513T>A
|
|
|
NM_001042472.3:c.824T>A
MANE Select
|
NP_001035937.1:p.Phe275Tyr
|
|
NM_015600.5:c.824T>A
|
NP_056415.1:p.Phe275Tyr
|
|