ENST00000527168.6:n.392G>C
|
|
|
ENST00000529110.2:c.377G>C
|
ENSP00000435349.2:p.Trp126Ser
|
|
ENST00000529957.6:n.351G>C
|
|
|
ENST00000683366.1:c.*25G>C
|
ENSP00000507283.1:n.*25G>C
|
|
ENST00000683887.1:c.341G>C
|
ENSP00000506886.1:p.Trp114Ser
|
|
ENST00000684100.1:n.287G>C
|
|
|
ENST00000684126.1:n.351G>C
|
|
|
ENST00000684688.1:n.918G>C
|
|
|
ENST00000204679.9:c.293G>C
MANE Select
|
ENSP00000204679.4:p.Trp98Ser
|
|
ENST00000204679.8:c.293G>C
|
ENSP00000204679.4:p.Trp98Ser
|
|
ENST00000526820.5:c.*195G>C
|
ENSP00000434413.1:n.*195G>C
|
|
ENST00000527076.1:n.1309G>C
|
|
|
ENST00000527168.5:n.329G>C
|
|
|
ENST00000529110.1:c.360G>C
|
|
|
ENST00000529957.5:n.392G>C
|
|
|
NM_032520.4:c.293G>C
|
NP_115909.1:p.Trp98Ser
|
|
XM_017023782.1:c.341G>C
|
XP_016879271.1:p.Trp114Ser
|
|
XM_017023783.1:c.-68G>C
|
XP_016879272.1:n.-68G>C
|
|
NM_032520.5:c.293G>C
MANE Select
|
NP_115909.1:p.Trp98Ser
|
|