ENST00000527168.6:n.858A>T
|
|
|
ENST00000529110.2:c.843A>T
|
ENSP00000435349.2:p.Ser281=
|
|
ENST00000529957.6:n.817A>T
|
|
|
ENST00000683366.1:c.*491A>T
|
ENSP00000507283.1:n.*491A>T
|
|
ENST00000683887.1:c.807A>T
|
ENSP00000506886.1:p.Ser269=
|
|
ENST00000684100.1:n.753A>T
|
|
|
ENST00000684126.1:n.893A>T
|
|
|
ENST00000684688.1:n.1384A>T
|
|
|
ENST00000204679.9:c.759A>T
MANE Select
|
ENSP00000204679.4:p.Ser253=
|
|
ENST00000204679.8:c.759A>T
|
ENSP00000204679.4:p.Ser253=
|
|
ENST00000527076.1:n.1982A>T
|
|
|
ENST00000527168.5:n.926A>T
|
|
|
ENST00000529957.5:n.858A>T
|
|
|
NM_032520.4:c.759A>T
|
NP_115909.1:p.Ser253=
|
|
XM_017023782.1:c.807A>T
|
XP_016879271.1:p.Ser269=
|
|
XM_017023783.1:c.399A>T
|
XP_016879272.1:p.Ser133=
|
|
NM_032520.5:c.759A>T
MANE Select
|
NP_115909.1:p.Ser253=
|
|