ENST00000455537.7:c.742G=
MANE Select
|
ENSP00000408979.2:p.Val248=
|
|
ENST00000674619.1:c.742G=
|
ENSP00000502270.1:p.Val248=
|
|
ENST00000676457.1:c.637G=
|
ENSP00000501588.1:p.Val213=
|
|
ENST00000286452.5:c.475G=
|
ENSP00000286452.5:p.Val159=
|
|
ENST00000455537.6:c.742G=
|
ENSP00000408979.2:p.Val248=
|
|
NM_004984.2:c.742G=
|
NP_004975.2:p.Val248=
|
|
NM_001354705.1:c.475G=
|
NP_001341634.1:p.Val159=
|
|
NM_004984.3:c.742G=
|
NP_004975.2:p.Val248=
|
|
XR_002957324.1:n.975G=
|
|
|
NM_004984.4:c.742G=
MANE Select
|
NP_004975.2:p.Val248=
|
|
NM_001354705.2:c.475G=
|
NP_001341634.1:p.Val159=
|
|