ENST00000463045.3:c.253G=
|
ENSP00000481376.2:p.Asp85=
|
|
ENST00000491274.6:c.382G=
|
ENSP00000480482.2:p.Asp128=
|
|
ENST00000375499.8:c.424G=
MANE Select
|
ENSP00000364649.3:p.Asp142=
|
|
ENST00000375499.7:c.424G=
|
ENSP00000364649.3:p.Asp142=
|
|
ENST00000463045.2:c.253G=
|
ENSP00000481376.1:p.Asp85=
|
|
ENST00000475506.1:n.341G=
|
|
|
ENST00000485515.5:n.358G=
|
|
|
ENST00000491274.5:c.382G=
|
ENSP00000480482.1:p.Asp128=
|
|
NM_003000.2:c.424G= , LRG_316t1:c.424G=
|
NP_002991.2:p.Asp142=
|
|
NM_003000.3:c.424G=
MANE Select
|
NP_002991.2:p.Asp142=
|
|