ENST00000297289.9:c.988G=
|
ENSP00000516619.1:p.Asp330=
|
|
ENST00000418964.2:c.2086G=
|
ENSP00000389424.2:p.Asp696=
|
|
ENST00000706906.1:c.*2055G=
|
ENSP00000516618.1:n.*2055G=
|
|
ENST00000308192.14:c.2035G=
MANE Select
|
ENSP00000308938.9:p.Asp679=
|
|
ENST00000308192.13:c.2035G=
|
ENSP00000308938.9:p.Asp679=
|
|
ENST00000461414.2:n.58G=
|
|
|
ENST00000467466.1:n.336G=
|
|
|
NM_000301.3:c.2035G= , LRG_571t1:c.2035G=
|
NP_000292.1:p.Asp679=
|
|
NM_000301.4:c.2035G=
|
NP_000292.1:p.Asp679=
|
|
NM_000301.5:c.2035G=
MANE Select
|
NP_000292.1:p.Asp679=
|
|