ENST00000527168.6:n.577G>T
|
|
|
ENST00000529110.2:c.562G>T
|
ENSP00000435349.2:p.Ala188Ser
|
|
ENST00000529957.6:n.536G>T
|
|
|
ENST00000683366.1:c.*210G>T
|
ENSP00000507283.1:n.*210G>T
|
|
ENST00000683887.1:c.526G>T
|
ENSP00000506886.1:p.Ala176Ser
|
|
ENST00000684100.1:n.472G>T
|
|
|
ENST00000684126.1:n.536G>T
|
|
|
ENST00000684688.1:n.1103G>T
|
|
|
ENST00000204679.9:c.478G>T
MANE Select
|
ENSP00000204679.4:p.Ala160Ser
|
|
ENST00000204679.8:c.478G>T
|
ENSP00000204679.4:p.Ala160Ser
|
|
ENST00000527076.1:n.1494G>T
|
|
|
ENST00000527168.5:n.514G>T
|
|
|
ENST00000529110.1:c.545G>T
|
|
|
ENST00000529957.5:n.577G>T
|
|
|
NM_032520.4:c.478G>T
|
NP_115909.1:p.Ala160Ser
|
|
XM_017023782.1:c.526G>T
|
XP_016879271.1:p.Ala176Ser
|
|
XM_017023783.1:c.118G>T
|
XP_016879272.1:p.Ala40Ser
|
|
NM_032520.5:c.478G>T
MANE Select
|
NP_115909.1:p.Ala160Ser
|
|