ENST00000394867.9:n.607C>G
|
|
|
ENST00000687128.1:n.607C>G
|
|
|
ENST00000262948.10:c.168C>G
MANE Select
|
ENSP00000262948.4:p.Ala56=
|
|
ENST00000262948.9:c.168C>G
|
ENSP00000262948.3:p.Ala56=
|
|
ENST00000394867.8:c.-124C>G
|
ENSP00000378336.1:n.-124C>G
|
|
ENST00000599345.1:n.365C>G
|
|
|
NM_030662.3:c.168C>G , LRG_750t1:c.168C>G
|
NP_109587.1:p.Ala56=
|
|
XM_006722799.2:c.168C>G
|
XP_006722862.1:p.Ala56=
|
|
XM_017026989.1:c.168C>G
|
XP_016882478.1:p.Ala56=
|
|
XM_017026990.1:c.168C>G
|
XP_016882479.1:p.Ala56=
|
|
XM_017026991.1:c.168C>G
|
XP_016882480.1:p.Ala56=
|
|
NM_030662.4:c.168C>G
MANE Select
|
NP_109587.1:p.Ala56=
|
|