ENST00000527168.6:n.566C>G
|
|
|
ENST00000529110.2:c.551C>G
|
ENSP00000435349.2:p.Thr184Ser
|
|
ENST00000529957.6:n.525C>G
|
|
|
ENST00000683366.1:c.*199C>G
|
ENSP00000507283.1:n.*199C>G
|
|
ENST00000683887.1:c.515C>G
|
ENSP00000506886.1:p.Thr172Ser
|
|
ENST00000684100.1:n.461C>G
|
|
|
ENST00000684126.1:n.525C>G
|
|
|
ENST00000684688.1:n.1092C>G
|
|
|
ENST00000204679.9:c.467C>G
MANE Select
|
ENSP00000204679.4:p.Thr156Ser
|
|
ENST00000204679.8:c.467C>G
|
ENSP00000204679.4:p.Thr156Ser
|
|
ENST00000527076.1:n.1483C>G
|
|
|
ENST00000527168.5:n.503C>G
|
|
|
ENST00000529110.1:c.534C>G
|
|
|
ENST00000529957.5:n.566C>G
|
|
|
NM_032520.4:c.467C>G
|
NP_115909.1:p.Thr156Ser
|
|
XM_017023782.1:c.515C>G
|
XP_016879271.1:p.Thr172Ser
|
|
XM_017023783.1:c.107C>G
|
XP_016879272.1:p.Thr36Ser
|
|
NM_032520.5:c.467C>G
MANE Select
|
NP_115909.1:p.Thr156Ser
|
|