ENST00000527168.6:n.391T>A
|
|
|
ENST00000529110.2:c.376T>A
|
ENSP00000435349.2:p.Trp126Arg
|
|
ENST00000529957.6:n.350T>A
|
|
|
ENST00000683366.1:c.*24T>A
|
ENSP00000507283.1:n.*24T>A
|
|
ENST00000683887.1:c.340T>A
|
ENSP00000506886.1:p.Trp114Arg
|
|
ENST00000684100.1:n.286T>A
|
|
|
ENST00000684126.1:n.350T>A
|
|
|
ENST00000684688.1:n.917T>A
|
|
|
ENST00000204679.9:c.292T>A
MANE Select
|
ENSP00000204679.4:p.Trp98Arg
|
|
ENST00000204679.8:c.292T>A
|
ENSP00000204679.4:p.Trp98Arg
|
|
ENST00000526820.5:c.*194T>A
|
ENSP00000434413.1:n.*194T>A
|
|
ENST00000527076.1:n.1308T>A
|
|
|
ENST00000527168.5:n.328T>A
|
|
|
ENST00000529110.1:c.359T>A
|
|
|
ENST00000529957.5:n.391T>A
|
|
|
NM_032520.4:c.292T>A
|
NP_115909.1:p.Trp98Arg
|
|
XM_017023782.1:c.340T>A
|
XP_016879271.1:p.Trp114Arg
|
|
XM_017023783.1:c.-69T>A
|
XP_016879272.1:n.-69T>A
|
|
NM_032520.5:c.292T>A
MANE Select
|
NP_115909.1:p.Trp98Arg
|
|