ENST00000527168.6:n.907T>C
|
|
|
ENST00000529110.2:c.892T>C
|
ENSP00000435349.2:p.Tyr298His
|
|
ENST00000529957.6:n.866T>C
|
|
|
ENST00000683366.1:c.*540T>C
|
ENSP00000507283.1:n.*540T>C
|
|
ENST00000683887.1:c.856T>C
|
ENSP00000506886.1:p.Tyr286His
|
|
ENST00000684100.1:n.802T>C
|
|
|
ENST00000684126.1:n.942T>C
|
|
|
ENST00000684688.1:n.1433T>C
|
|
|
ENST00000204679.9:c.808T>C
MANE Select
|
ENSP00000204679.4:p.Tyr270His
|
|
ENST00000204679.8:c.808T>C
|
ENSP00000204679.4:p.Tyr270His
|
|
ENST00000527076.1:n.2031T>C
|
|
|
ENST00000527168.5:n.975T>C
|
|
|
ENST00000529957.5:n.907T>C
|
|
|
NM_032520.4:c.808T>C
|
NP_115909.1:p.Tyr270His
|
|
XM_017023782.1:c.856T>C
|
XP_016879271.1:p.Tyr286His
|
|
XM_017023783.1:c.448T>C
|
XP_016879272.1:p.Tyr150His
|
|
NM_032520.5:c.808T>C
MANE Select
|
NP_115909.1:p.Tyr270His
|
|