ENST00000527168.6:n.540G>C
|
|
|
ENST00000529110.2:c.525G>C
|
ENSP00000435349.2:p.Arg175=
|
|
ENST00000529957.6:n.499G>C
|
|
|
ENST00000683366.1:c.*173G>C
|
ENSP00000507283.1:n.*173G>C
|
|
ENST00000683887.1:c.489G>C
|
ENSP00000506886.1:p.Arg163=
|
|
ENST00000684100.1:n.435G>C
|
|
|
ENST00000684126.1:n.499G>C
|
|
|
ENST00000684688.1:n.1066G>C
|
|
|
ENST00000204679.9:c.441G>C
MANE Select
|
ENSP00000204679.4:p.Arg147=
|
|
ENST00000204679.8:c.441G>C
|
ENSP00000204679.4:p.Arg147=
|
|
ENST00000527076.1:n.1457G>C
|
|
|
ENST00000527168.5:n.477G>C
|
|
|
ENST00000529110.1:c.508G>C
|
|
|
ENST00000529957.5:n.540G>C
|
|
|
NM_032520.4:c.441G>C
|
NP_115909.1:p.Arg147=
|
|
XM_017023782.1:c.489G>C
|
XP_016879271.1:p.Arg163=
|
|
XM_017023783.1:c.81G>C
|
XP_016879272.1:p.Arg27=
|
|
NM_032520.5:c.441G>C
MANE Select
|
NP_115909.1:p.Arg147=
|
|