ENST00000527168.6:n.696G>C
|
|
|
ENST00000529110.2:c.681G>C
|
ENSP00000435349.2:p.Leu227=
|
|
ENST00000529957.6:n.655G>C
|
|
|
ENST00000683366.1:c.*329G>C
|
ENSP00000507283.1:n.*329G>C
|
|
ENST00000683887.1:c.645G>C
|
ENSP00000506886.1:p.Leu215=
|
|
ENST00000684100.1:n.591G>C
|
|
|
ENST00000684126.1:n.655G>C
|
|
|
ENST00000684688.1:n.1222G>C
|
|
|
ENST00000204679.9:c.597G>C
MANE Select
|
ENSP00000204679.4:p.Leu199=
|
|
ENST00000204679.8:c.597G>C
|
ENSP00000204679.4:p.Leu199=
|
|
ENST00000527076.1:n.1744G>C
|
|
|
ENST00000527168.5:n.764G>C
|
|
|
ENST00000529957.5:n.696G>C
|
|
|
NM_032520.4:c.597G>C
|
NP_115909.1:p.Leu199=
|
|
XM_017023782.1:c.645G>C
|
XP_016879271.1:p.Leu215=
|
|
XM_017023783.1:c.237G>C
|
XP_016879272.1:p.Leu79=
|
|
NM_032520.5:c.597G>C
MANE Select
|
NP_115909.1:p.Leu199=
|
|