ENST00000527168.6:n.910A>T
|
|
|
ENST00000529110.2:c.895A>T
|
ENSP00000435349.2:p.Thr299Ser
|
|
ENST00000529957.6:n.869A>T
|
|
|
ENST00000683366.1:c.*543A>T
|
ENSP00000507283.1:n.*543A>T
|
|
ENST00000683887.1:c.859A>T
|
ENSP00000506886.1:p.Thr287Ser
|
|
ENST00000684100.1:n.805A>T
|
|
|
ENST00000684126.1:n.945A>T
|
|
|
ENST00000684688.1:n.1436A>T
|
|
|
ENST00000204679.9:c.811A>T
MANE Select
|
ENSP00000204679.4:p.Thr271Ser
|
|
ENST00000204679.8:c.811A>T
|
ENSP00000204679.4:p.Thr271Ser
|
|
ENST00000527076.1:n.2034A>T
|
|
|
ENST00000527168.5:n.978A>T
|
|
|
ENST00000529957.5:n.910A>T
|
|
|
NM_032520.4:c.811A>T
|
NP_115909.1:p.Thr271Ser
|
|
XM_017023782.1:c.859A>T
|
XP_016879271.1:p.Thr287Ser
|
|
XM_017023783.1:c.451A>T
|
XP_016879272.1:p.Thr151Ser
|
|
NM_032520.5:c.811A>T
MANE Select
|
NP_115909.1:p.Thr271Ser
|
|