ENST00000527168.6:n.593C>G
|
|
|
ENST00000529110.2:c.578C>G
|
ENSP00000435349.2:p.Thr193Ser
|
|
ENST00000529957.6:n.552C>G
|
|
|
ENST00000683366.1:c.*226C>G
|
ENSP00000507283.1:n.*226C>G
|
|
ENST00000683887.1:c.542C>G
|
ENSP00000506886.1:p.Thr181Ser
|
|
ENST00000684100.1:n.488C>G
|
|
|
ENST00000684126.1:n.552C>G
|
|
|
ENST00000684688.1:n.1119C>G
|
|
|
ENST00000204679.9:c.494C>G
MANE Select
|
ENSP00000204679.4:p.Thr165Ser
|
|
ENST00000204679.8:c.494C>G
|
ENSP00000204679.4:p.Thr165Ser
|
|
ENST00000527076.1:n.1510C>G
|
|
|
ENST00000527168.5:n.530C>G
|
|
|
ENST00000529957.5:n.593C>G
|
|
|
NM_032520.4:c.494C>G
|
NP_115909.1:p.Thr165Ser
|
|
XM_017023782.1:c.542C>G
|
XP_016879271.1:p.Thr181Ser
|
|
XM_017023783.1:c.134C>G
|
XP_016879272.1:p.Thr45Ser
|
|
NM_032520.5:c.494C>G
MANE Select
|
NP_115909.1:p.Thr165Ser
|
|