ENST00000225964.10:c.4338C>T
MANE Select
|
ENSP00000225964.6:p.Asp1446=
|
|
ENST00000225964.9:c.4338C>T
|
ENSP00000225964.5:p.Asp1446=
|
|
NM_000088.3:c.4338C>T , LRG_1t1:c.4338C>T
|
NP_000079.2:p.Asp1446=
|
|
XM_005257058.3:c.4068C>T
|
XP_005257115.2:p.Asp1356=
|
|
XM_005257059.3:c.3420C>T
|
XP_005257116.2:p.Asp1140=
|
|
XM_011524341.1:c.4140C>T
|
XP_011522643.1:p.Asp1380=
|
|
XM_005257058.4:c.4068C>T
|
XP_005257115.2:p.Asp1356=
|
|
XM_005257059.4:c.3420C>T
|
XP_005257116.2:p.Asp1140=
|
|
NM_000088.4:c.4338C>T
MANE Select
|
NP_000079.2:p.Asp1446=
|
|