ENST00000527168.6:n.750C>T
|
|
|
ENST00000529110.2:c.735C>T
|
ENSP00000435349.2:p.Gly245=
|
|
ENST00000529957.6:n.709C>T
|
|
|
ENST00000683366.1:c.*383C>T
|
ENSP00000507283.1:n.*383C>T
|
|
ENST00000683887.1:c.699C>T
|
ENSP00000506886.1:p.Gly233=
|
|
ENST00000684100.1:n.645C>T
|
|
|
ENST00000684126.1:n.785C>T
|
|
|
ENST00000684688.1:n.1276C>T
|
|
|
ENST00000204679.9:c.651C>T
MANE Select
|
ENSP00000204679.4:p.Gly217=
|
|
ENST00000204679.8:c.651C>T
|
ENSP00000204679.4:p.Gly217=
|
|
ENST00000527076.1:n.1874C>T
|
|
|
ENST00000527168.5:n.818C>T
|
|
|
ENST00000529957.5:n.750C>T
|
|
|
NM_032520.4:c.651C>T
|
NP_115909.1:p.Gly217=
|
|
XM_017023782.1:c.699C>T
|
XP_016879271.1:p.Gly233=
|
|
XM_017023783.1:c.291C>T
|
XP_016879272.1:p.Gly97=
|
|
NM_032520.5:c.651C>T
MANE Select
|
NP_115909.1:p.Gly217=
|
|