ENST00000225964.10:c.4353C>T
MANE Select
|
ENSP00000225964.6:p.Asp1451=
|
|
ENST00000225964.9:c.4353C>T
|
ENSP00000225964.5:p.Asp1451=
|
|
NM_000088.3:c.4353C>T , LRG_1t1:c.4353C>T
|
NP_000079.2:p.Asp1451=
|
|
XM_005257058.3:c.4083C>T
|
XP_005257115.2:p.Asp1361=
|
|
XM_005257059.3:c.3435C>T
|
XP_005257116.2:p.Asp1145=
|
|
XM_011524341.1:c.4155C>T
|
XP_011522643.1:p.Asp1385=
|
|
XM_005257058.4:c.4083C>T
|
XP_005257115.2:p.Asp1361=
|
|
XM_005257059.4:c.3435C>T
|
XP_005257116.2:p.Asp1145=
|
|
NM_000088.4:c.4353C>T
MANE Select
|
NP_000079.2:p.Asp1451=
|
|