ENST00000527168.6:n.365T>A
|
|
|
ENST00000529110.2:c.350T>A
|
ENSP00000435349.2:p.Val117Glu
|
|
ENST00000529957.6:n.324T>A
|
|
|
ENST00000683366.1:c.211T>A
|
ENSP00000507283.1:p.Ter71Arg
|
|
ENST00000683887.1:c.314T>A
|
ENSP00000506886.1:p.Val105Glu
|
|
ENST00000684100.1:n.260T>A
|
|
|
ENST00000684126.1:n.324T>A
|
|
|
ENST00000684688.1:n.891T>A
|
|
|
ENST00000204679.9:c.266T>A
MANE Select
|
ENSP00000204679.4:p.Val89Glu
|
|
ENST00000204679.8:c.266T>A
|
ENSP00000204679.4:p.Val89Glu
|
|
ENST00000526820.5:c.*168T>A
|
ENSP00000434413.1:n.*168T>A
|
|
ENST00000527076.1:n.1282T>A
|
|
|
ENST00000527168.5:n.302T>A
|
|
|
ENST00000529110.1:c.333T>A
|
|
|
ENST00000529957.5:n.365T>A
|
|
|
NM_032520.4:c.266T>A
|
NP_115909.1:p.Val89Glu
|
|
XM_017023782.1:c.314T>A
|
XP_016879271.1:p.Val105Glu
|
|
XM_017023783.1:c.-95T>A
|
XP_016879272.1:n.-95T>A
|
|
NM_032520.5:c.266T>A
MANE Select
|
NP_115909.1:p.Val89Glu
|
|