ENST00000225964.10:c.1062A>G
MANE Select
|
ENSP00000225964.6:p.Glu354=
|
|
ENST00000225964.9:c.1062A>G
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ENSP00000225964.5:p.Glu354=
|
|
ENST00000471344.1:n.6A>G
|
|
|
NM_000088.3:c.1062A>G , LRG_1t1:c.1062A>G
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NP_000079.2:p.Glu354=
|
|
XM_005257058.3:c.1062A>G
|
XP_005257115.2:p.Glu354=
|
|
XM_005257059.3:c.957+654A>G
|
XP_005257116.2:n.957+654A>G
|
|
XM_011524341.1:c.958-182A>G
|
XP_011522643.1:n.958-182A>G
|
|
XM_005257058.4:c.1062A>G
|
XP_005257115.2:p.Glu354=
|
|
XM_005257059.4:c.957+654A>G
|
XP_005257116.2:n.957+654A>G
|
|
NM_000088.4:c.1062A>G
MANE Select
|
NP_000079.2:p.Glu354=
|
|