ENST00000225964.10:c.4305C>T
MANE Select
|
ENSP00000225964.6:p.Ser1435=
|
|
ENST00000225964.9:c.4305C>T
|
ENSP00000225964.5:p.Ser1435=
|
|
NM_000088.3:c.4305C>T , LRG_1t1:c.4305C>T
|
NP_000079.2:p.Ser1435=
|
|
XM_005257058.3:c.4035C>T
|
XP_005257115.2:p.Ser1345=
|
|
XM_005257059.3:c.3387C>T
|
XP_005257116.2:p.Ser1129=
|
|
XM_011524341.1:c.4107C>T
|
XP_011522643.1:p.Ser1369=
|
|
XM_005257058.4:c.4035C>T
|
XP_005257115.2:p.Ser1345=
|
|
XM_005257059.4:c.3387C>T
|
XP_005257116.2:p.Ser1129=
|
|
NM_000088.4:c.4305C>T
MANE Select
|
NP_000079.2:p.Ser1435=
|
|