ENST00000463045.3:c.315A=
|
ENSP00000481376.2:p.Glu105=
|
|
ENST00000491274.6:c.444A=
|
ENSP00000480482.2:p.Glu148=
|
|
ENST00000375499.8:c.486A=
MANE Select
|
ENSP00000364649.3:p.Glu162=
|
|
ENST00000375499.7:c.486A=
|
ENSP00000364649.3:p.Glu162=
|
|
ENST00000463045.2:c.315A=
|
ENSP00000481376.1:p.Glu105=
|
|
ENST00000475506.1:n.403A=
|
|
|
ENST00000485515.5:n.420A=
|
|
|
ENST00000491274.5:c.444A=
|
ENSP00000480482.1:p.Glu148=
|
|
NM_003000.2:c.486A= , LRG_316t1:c.486A=
|
NP_002991.2:p.Glu162=
|
|
NM_003000.3:c.486A=
MANE Select
|
NP_002991.2:p.Glu162=
|
|