ENST00000527168.6:n.605G>T
|
|
|
ENST00000529110.2:c.590G>T
|
ENSP00000435349.2:p.Cys197Phe
|
|
ENST00000529957.6:n.564G>T
|
|
|
ENST00000683366.1:c.*238G>T
|
ENSP00000507283.1:n.*238G>T
|
|
ENST00000683887.1:c.554G>T
|
ENSP00000506886.1:p.Cys185Phe
|
|
ENST00000684100.1:n.500G>T
|
|
|
ENST00000684126.1:n.564G>T
|
|
|
ENST00000684688.1:n.1131G>T
|
|
|
ENST00000204679.9:c.506G>T
MANE Select
|
ENSP00000204679.4:p.Cys169Phe
|
|
ENST00000204679.8:c.506G>T
|
ENSP00000204679.4:p.Cys169Phe
|
|
ENST00000527076.1:n.1522G>T
|
|
|
ENST00000527168.5:n.542G>T
|
|
|
ENST00000529957.5:n.605G>T
|
|
|
NM_032520.4:c.506G>T
|
NP_115909.1:p.Cys169Phe
|
|
XM_017023782.1:c.554G>T
|
XP_016879271.1:p.Cys185Phe
|
|
XM_017023783.1:c.146G>T
|
XP_016879272.1:p.Cys49Phe
|
|
NM_032520.5:c.506G>T
MANE Select
|
NP_115909.1:p.Cys169Phe
|
|