ENST00000455537.7:c.744G>A
MANE Select
|
ENSP00000408979.2:p.Val248=
|
|
ENST00000674619.1:c.744G>A
|
ENSP00000502270.1:p.Val248=
|
|
ENST00000676457.1:c.639G>A
|
ENSP00000501588.1:p.Val213=
|
|
ENST00000286452.5:c.477G>A
|
ENSP00000286452.5:p.Val159=
|
|
ENST00000455537.6:c.744G>A
|
ENSP00000408979.2:p.Val248=
|
|
NM_004984.2:c.744G>A
|
NP_004975.2:p.Val248=
|
|
NM_001354705.1:c.477G>A
|
NP_001341634.1:p.Val159=
|
|
NM_004984.3:c.744G>A
|
NP_004975.2:p.Val248=
|
|
XR_002957324.1:n.977G>A
|
|
|
NM_004984.4:c.744G>A
MANE Select
|
NP_004975.2:p.Val248=
|
|
NM_001354705.2:c.477G>A
|
NP_001341634.1:p.Val159=
|
|