ENST00000225964.10:c.3195T>G
MANE Select
|
ENSP00000225964.6:p.Asp1065Glu
|
|
ENST00000225964.9:c.3195T>G
|
ENSP00000225964.5:p.Asp1065Glu
|
|
ENST00000486572.1:n.13T>G
|
|
|
ENST00000511732.1:n.139T>G
|
|
|
NM_000088.3:c.3195T>G , LRG_1t1:c.3195T>G
|
NP_000079.2:p.Asp1065Glu
|
|
XM_005257058.3:c.2925T>G
|
XP_005257115.2:p.Asp975Glu
|
|
XM_005257059.3:c.2277T>G
|
XP_005257116.2:p.Asp759Glu
|
|
XM_011524341.1:c.2997T>G
|
XP_011522643.1:p.Asp999Glu
|
|
XM_005257058.4:c.2925T>G
|
XP_005257115.2:p.Asp975Glu
|
|
XM_005257059.4:c.2277T>G
|
XP_005257116.2:p.Asp759Glu
|
|
NM_000088.4:c.3195T>G
MANE Select
|
NP_000079.2:p.Asp1065Glu
|
|