ENST00000527168.6:n.829A>T
|
|
|
ENST00000529110.2:c.814A>T
|
ENSP00000435349.2:p.Asn272Tyr
|
|
ENST00000529957.6:n.788A>T
|
|
|
ENST00000683366.1:c.*462A>T
|
ENSP00000507283.1:n.*462A>T
|
|
ENST00000683887.1:c.778A>T
|
ENSP00000506886.1:p.Asn260Tyr
|
|
ENST00000684100.1:n.724A>T
|
|
|
ENST00000684126.1:n.864A>T
|
|
|
ENST00000684688.1:n.1355A>T
|
|
|
ENST00000204679.9:c.730A>T
MANE Select
|
ENSP00000204679.4:p.Asn244Tyr
|
|
ENST00000204679.8:c.730A>T
|
ENSP00000204679.4:p.Asn244Tyr
|
|
ENST00000527076.1:n.1953A>T
|
|
|
ENST00000527168.5:n.897A>T
|
|
|
ENST00000529957.5:n.829A>T
|
|
|
NM_032520.4:c.730A>T
|
NP_115909.1:p.Asn244Tyr
|
|
XM_017023782.1:c.778A>T
|
XP_016879271.1:p.Asn260Tyr
|
|
XM_017023783.1:c.370A>T
|
XP_016879272.1:p.Asn124Tyr
|
|
NM_032520.5:c.730A>T
MANE Select
|
NP_115909.1:p.Asn244Tyr
|
|