ENST00000527168.6:n.844C>T
|
|
|
ENST00000529110.2:c.829C>T
|
ENSP00000435349.2:p.His277Tyr
|
|
ENST00000529957.6:n.803C>T
|
|
|
ENST00000683366.1:c.*477C>T
|
ENSP00000507283.1:n.*477C>T
|
|
ENST00000683887.1:c.793C>T
|
ENSP00000506886.1:p.His265Tyr
|
|
ENST00000684100.1:n.739C>T
|
|
|
ENST00000684126.1:n.879C>T
|
|
|
ENST00000684688.1:n.1370C>T
|
|
|
ENST00000204679.9:c.745C>T
MANE Select
|
ENSP00000204679.4:p.His249Tyr
|
|
ENST00000204679.8:c.745C>T
|
ENSP00000204679.4:p.His249Tyr
|
|
ENST00000527076.1:n.1968C>T
|
|
|
ENST00000527168.5:n.912C>T
|
|
|
ENST00000529957.5:n.844C>T
|
|
|
NM_032520.4:c.745C>T
|
NP_115909.1:p.His249Tyr
|
|
XM_017023782.1:c.793C>T
|
XP_016879271.1:p.His265Tyr
|
|
XM_017023783.1:c.385C>T
|
XP_016879272.1:p.His129Tyr
|
|
NM_032520.5:c.745C>T
MANE Select
|
NP_115909.1:p.His249Tyr
|
|