ENST00000321612.8:c.2137G=
MANE Select
|
ENSP00000370737.4:p.Val713=
|
|
ENST00000638233.1:n.572G=
|
|
|
ENST00000638661.1:c.337G=
|
ENSP00000491369.1:p.Val113=
|
|
ENST00000638694.1:n.324G=
|
|
|
ENST00000639318.1:c.337G=
|
ENSP00000491932.1:p.Val113=
|
|
ENST00000639364.1:n.1837G=
|
|
|
ENST00000639443.1:n.1705G=
|
|
|
ENST00000639954.1:n.1845G=
|
|
|
ENST00000640505.1:n.376G=
|
|
|
ENST00000321612.6:c.2137G=
|
ENSP00000370737.3:p.Val713=
|
|
NM_000170.2:c.2137G= , LRG_643t1:c.2137G=
|
NP_000161.2:p.Val713=
|
|
NM_000170.3:c.2137G=
MANE Select
|
NP_000161.2:p.Val713=
|
|