ENST00000463045.3:c.363G=
|
ENSP00000481376.2:p.Glu121=
|
|
ENST00000491274.6:c.492G=
|
ENSP00000480482.2:p.Glu164=
|
|
ENST00000375499.8:c.534G=
MANE Select
|
ENSP00000364649.3:p.Glu178=
|
|
ENST00000375499.7:c.534G=
|
ENSP00000364649.3:p.Glu178=
|
|
ENST00000463045.2:c.363G=
|
ENSP00000481376.1:p.Glu121=
|
|
ENST00000475506.1:n.451G=
|
|
|
ENST00000485515.5:n.468G=
|
|
|
ENST00000491274.5:c.492G=
|
ENSP00000480482.1:p.Glu164=
|
|
NM_003000.2:c.534G= , LRG_316t1:c.534G=
|
NP_002991.2:p.Glu178=
|
|
NM_003000.3:c.534G=
MANE Select
|
NP_002991.2:p.Glu178=
|
|