ENST00000527168.6:n.435G>C
|
|
|
ENST00000529110.2:c.420G>C
|
ENSP00000435349.2:p.Glu140Asp
|
|
ENST00000529957.6:n.394G>C
|
|
|
ENST00000683366.1:c.*68G>C
|
ENSP00000507283.1:n.*68G>C
|
|
ENST00000683887.1:c.384G>C
|
ENSP00000506886.1:p.Glu128Asp
|
|
ENST00000684100.1:n.330G>C
|
|
|
ENST00000684126.1:n.394G>C
|
|
|
ENST00000684688.1:n.961G>C
|
|
|
ENST00000204679.9:c.336G>C
MANE Select
|
ENSP00000204679.4:p.Glu112Asp
|
|
ENST00000204679.8:c.336G>C
|
ENSP00000204679.4:p.Glu112Asp
|
|
ENST00000526820.5:c.*238G>C
|
ENSP00000434413.1:n.*238G>C
|
|
ENST00000527076.1:n.1352G>C
|
|
|
ENST00000527168.5:n.372G>C
|
|
|
ENST00000529110.1:c.403G>C
|
|
|
ENST00000529957.5:n.435G>C
|
|
|
NM_032520.4:c.336G>C
|
NP_115909.1:p.Glu112Asp
|
|
XM_017023782.1:c.384G>C
|
XP_016879271.1:p.Glu128Asp
|
|
XM_017023783.1:c.-25G>C
|
XP_016879272.1:n.-25G>C
|
|
NM_032520.5:c.336G>C
MANE Select
|
NP_115909.1:p.Glu112Asp
|
|