ENST00000527168.6:n.862G>T
|
|
|
ENST00000529110.2:c.847G>T
|
ENSP00000435349.2:p.Glu283Ter
|
|
ENST00000529957.6:n.821G>T
|
|
|
ENST00000683366.1:c.*495G>T
|
ENSP00000507283.1:n.*495G>T
|
|
ENST00000683887.1:c.811G>T
|
ENSP00000506886.1:p.Glu271Ter
|
|
ENST00000684100.1:n.757G>T
|
|
|
ENST00000684126.1:n.897G>T
|
|
|
ENST00000684688.1:n.1388G>T
|
|
|
ENST00000204679.9:c.763G>T
MANE Select
|
ENSP00000204679.4:p.Glu255Ter
|
|
ENST00000204679.8:c.763G>T
|
ENSP00000204679.4:p.Glu255Ter
|
|
ENST00000527076.1:n.1986G>T
|
|
|
ENST00000527168.5:n.930G>T
|
|
|
ENST00000529957.5:n.862G>T
|
|
|
NM_032520.4:c.763G>T
|
NP_115909.1:p.Glu255Ter
|
|
XM_017023782.1:c.811G>T
|
XP_016879271.1:p.Glu271Ter
|
|
XM_017023783.1:c.403G>T
|
XP_016879272.1:p.Glu135Ter
|
|
NM_032520.5:c.763G>T
MANE Select
|
NP_115909.1:p.Glu255Ter
|
|