ENST00000527168.6:n.627G>C
|
|
|
ENST00000529110.2:c.612G>C
|
ENSP00000435349.2:p.Val204=
|
|
ENST00000529957.6:n.586G>C
|
|
|
ENST00000683366.1:c.*260G>C
|
ENSP00000507283.1:n.*260G>C
|
|
ENST00000683887.1:c.576G>C
|
ENSP00000506886.1:p.Val192=
|
|
ENST00000684100.1:n.522G>C
|
|
|
ENST00000684126.1:n.586G>C
|
|
|
ENST00000684688.1:n.1153G>C
|
|
|
ENST00000204679.9:c.528G>C
MANE Select
|
ENSP00000204679.4:p.Val176=
|
|
ENST00000204679.8:c.528G>C
|
ENSP00000204679.4:p.Val176=
|
|
ENST00000527076.1:n.1675G>C
|
|
|
ENST00000527168.5:n.695G>C
|
|
|
ENST00000529957.5:n.627G>C
|
|
|
NM_032520.4:c.528G>C
|
NP_115909.1:p.Val176=
|
|
XM_017023782.1:c.576G>C
|
XP_016879271.1:p.Val192=
|
|
XM_017023783.1:c.168G>C
|
XP_016879272.1:p.Val56=
|
|
NM_032520.5:c.528G>C
MANE Select
|
NP_115909.1:p.Val176=
|
|