ENST00000527168.6:n.635C>G
|
|
|
ENST00000529110.2:c.620C>G
|
ENSP00000435349.2:p.Thr207Ser
|
|
ENST00000529957.6:n.594C>G
|
|
|
ENST00000683366.1:c.*268C>G
|
ENSP00000507283.1:n.*268C>G
|
|
ENST00000683887.1:c.584C>G
|
ENSP00000506886.1:p.Thr195Ser
|
|
ENST00000684100.1:n.530C>G
|
|
|
ENST00000684126.1:n.594C>G
|
|
|
ENST00000684688.1:n.1161C>G
|
|
|
ENST00000204679.9:c.536C>G
MANE Select
|
ENSP00000204679.4:p.Thr179Ser
|
|
ENST00000204679.8:c.536C>G
|
ENSP00000204679.4:p.Thr179Ser
|
|
ENST00000527076.1:n.1683C>G
|
|
|
ENST00000527168.5:n.703C>G
|
|
|
ENST00000529957.5:n.635C>G
|
|
|
NM_032520.4:c.536C>G
|
NP_115909.1:p.Thr179Ser
|
|
XM_017023782.1:c.584C>G
|
XP_016879271.1:p.Thr195Ser
|
|
XM_017023783.1:c.176C>G
|
XP_016879272.1:p.Thr59Ser
|
|
NM_032520.5:c.536C>G
MANE Select
|
NP_115909.1:p.Thr179Ser
|
|