ENST00000527168.6:n.556G>C
|
|
|
ENST00000529110.2:c.541G>C
|
ENSP00000435349.2:p.Glu181Gln
|
|
ENST00000529957.6:n.515G>C
|
|
|
ENST00000683366.1:c.*189G>C
|
ENSP00000507283.1:n.*189G>C
|
|
ENST00000683887.1:c.505G>C
|
ENSP00000506886.1:p.Glu169Gln
|
|
ENST00000684100.1:n.451G>C
|
|
|
ENST00000684126.1:n.515G>C
|
|
|
ENST00000684688.1:n.1082G>C
|
|
|
ENST00000204679.9:c.457G>C
MANE Select
|
ENSP00000204679.4:p.Glu153Gln
|
|
ENST00000204679.8:c.457G>C
|
ENSP00000204679.4:p.Glu153Gln
|
|
ENST00000527076.1:n.1473G>C
|
|
|
ENST00000527168.5:n.493G>C
|
|
|
ENST00000529110.1:c.524G>C
|
|
|
ENST00000529957.5:n.556G>C
|
|
|
NM_032520.4:c.457G>C
|
NP_115909.1:p.Glu153Gln
|
|
XM_017023782.1:c.505G>C
|
XP_016879271.1:p.Glu169Gln
|
|
XM_017023783.1:c.97G>C
|
XP_016879272.1:p.Glu33Gln
|
|
NM_032520.5:c.457G>C
MANE Select
|
NP_115909.1:p.Glu153Gln
|
|