ENST00000578493.2:n.798C>A
|
|
|
ENST00000699291.1:c.590C>A
|
ENSP00000514272.1:n.590C>A
|
|
ENST00000699292.1:n.505C>A
|
|
|
ENST00000225275.4:c.1465C>A
MANE Select
|
ENSP00000225275.3:p.Arg489Ser
|
|
ENST00000225275.3:c.1465C>A
|
ENSP00000225275.3:p.Arg489Ser
|
|
NM_000250.1:c.1465C>A , LRG_84t1:c.1465C>A
|
NP_000241.1:p.Arg489Ser
|
|
XM_011524821.1:c.1651C>A
|
XP_011523123.1:p.Arg551Ser
|
|
XM_011524822.1:c.1180C>A
|
XP_011523124.1:p.Arg394Ser
|
|
XM_011524823.1:c.*14C>A
|
XP_011523125.1:n.*14C>A
|
|
NM_000250.2:c.1465C>A
MANE Select
|
NP_000241.1:p.Arg489Ser
|
|