|
NM_002872.5:c.169G=
MANE Select
|
NP_002863.1:p.Asp57=
|
|
ENST00000249071.11:c.169G=
MANE Select
|
ENSP00000249071.6:p.Asp57=
|
|
NM_002872.4:c.169G=
|
NP_002863.1:p.Asp57=
|
|
ENST00000249071.10:c.169G=
|
ENSP00000249071.6:p.Asp57=
|
|
ENST00000405484.5:c.148G=
|
ENSP00000385590.1:p.Asp50=
|
|
ENST00000406508.5:c.37G=
|
ENSP00000385270.1:p.Asp13=
|
|
ENST00000441619.5:c.169G=
|
ENSP00000403778.1:p.Asp57=
|
|
ENST00000469532.1:n.299G=
|
|
|
ENST00000699915.1:n.227G=
|
|
|
XM_006724286.2:c.169G=
|
XP_006724349.1:p.Asp57=
|
|
XM_006724286.3:c.169G=
|
XP_006724349.1:p.Asp57=
|