ENST00000225964.10:c.990T>G
MANE Select
|
ENSP00000225964.6:p.Ala330=
|
|
ENST00000225964.9:c.990T>G
|
ENSP00000225964.5:p.Ala330=
|
|
ENST00000485870.1:n.315T>G
|
|
|
NM_000088.3:c.990T>G , LRG_1t1:c.990T>G
|
NP_000079.2:p.Ala330=
|
|
XM_005257058.3:c.990T>G
|
XP_005257115.2:p.Ala330=
|
|
XM_005257059.3:c.957+147T>G
|
XP_005257116.2:n.957+147T>G
|
|
XM_011524341.1:c.957+147T>G
|
XP_011522643.1:n.957+147T>G
|
|
XM_005257058.4:c.990T>G
|
XP_005257115.2:p.Ala330=
|
|
XM_005257059.4:c.957+147T>G
|
XP_005257116.2:n.957+147T>G
|
|
NM_000088.4:c.990T>G
MANE Select
|
NP_000079.2:p.Ala330=
|
|