ENST00000527168.6:n.592A>G
|
|
|
ENST00000529110.2:c.577A>G
|
ENSP00000435349.2:p.Thr193Ala
|
|
ENST00000529957.6:n.551A>G
|
|
|
ENST00000683366.1:c.*225A>G
|
ENSP00000507283.1:n.*225A>G
|
|
ENST00000683887.1:c.541A>G
|
ENSP00000506886.1:p.Thr181Ala
|
|
ENST00000684100.1:n.487A>G
|
|
|
ENST00000684126.1:n.551A>G
|
|
|
ENST00000684688.1:n.1118A>G
|
|
|
ENST00000204679.9:c.493A>G
MANE Select
|
ENSP00000204679.4:p.Thr165Ala
|
|
ENST00000204679.8:c.493A>G
|
ENSP00000204679.4:p.Thr165Ala
|
|
ENST00000527076.1:n.1509A>G
|
|
|
ENST00000527168.5:n.529A>G
|
|
|
ENST00000529957.5:n.592A>G
|
|
|
NM_032520.4:c.493A>G
|
NP_115909.1:p.Thr165Ala
|
|
XM_017023782.1:c.541A>G
|
XP_016879271.1:p.Thr181Ala
|
|
XM_017023783.1:c.133A>G
|
XP_016879272.1:p.Thr45Ala
|
|
NM_032520.5:c.493A>G
MANE Select
|
NP_115909.1:p.Thr165Ala
|
|