ENST00000527168.6:n.457G>T
|
|
|
ENST00000529110.2:c.442G>T
|
ENSP00000435349.2:p.Gly148Cys
|
|
ENST00000529957.6:n.416G>T
|
|
|
ENST00000683366.1:c.*90G>T
|
ENSP00000507283.1:n.*90G>T
|
|
ENST00000683887.1:c.406G>T
|
ENSP00000506886.1:p.Gly136Cys
|
|
ENST00000684100.1:n.352G>T
|
|
|
ENST00000684126.1:n.416G>T
|
|
|
ENST00000684688.1:n.983G>T
|
|
|
ENST00000204679.9:c.358G>T
MANE Select
|
ENSP00000204679.4:p.Gly120Cys
|
|
ENST00000204679.8:c.358G>T
|
ENSP00000204679.4:p.Gly120Cys
|
|
ENST00000526820.5:c.*260G>T
|
ENSP00000434413.1:n.*260G>T
|
|
ENST00000527076.1:n.1374G>T
|
|
|
ENST00000527168.5:n.394G>T
|
|
|
ENST00000529110.1:c.425G>T
|
|
|
ENST00000529957.5:n.457G>T
|
|
|
NM_032520.4:c.358G>T
|
NP_115909.1:p.Gly120Cys
|
|
XM_017023782.1:c.406G>T
|
XP_016879271.1:p.Gly136Cys
|
|
XM_017023783.1:c.-3G>T
|
XP_016879272.1:n.-3G>T
|
|
NM_032520.5:c.358G>T
MANE Select
|
NP_115909.1:p.Gly120Cys
|
|