ENST00000281928.9:c.3459C>T
MANE Select
|
ENSP00000281928.3:p.Ser1153=
|
|
ENST00000549786.2:c.2887C>T
|
|
|
ENST00000648379.1:n.1827C>T
|
|
|
ENST00000648737.1:n.3223C>T
|
|
|
ENST00000648825.1:n.199C>T
|
|
|
ENST00000648916.1:n.1470C>T
|
|
|
ENST00000649607.1:c.1643C>T
|
|
|
ENST00000650226.1:c.3459C>T
|
ENSP00000496981.1:p.Ser1153=
|
|
ENST00000281928.7:c.3459C>T
|
ENSP00000281928.3:p.Ser1153=
|
|
NM_015335.4:c.3459C>T
|
NP_056150.1:p.Ser1153=
|
|
XM_011538080.1:c.3459C>T
|
XP_011536382.1:p.Ser1153=
|
|
XM_011538081.1:c.3456C>T
|
XP_011536383.1:p.Ser1152=
|
|
XM_011538082.1:c.3429C>T
|
XP_011536384.1:p.Ser1143=
|
|
XM_011538080.2:c.3459C>T
|
XP_011536382.1:p.Ser1153=
|
|
XM_011538081.2:c.3456C>T
|
XP_011536383.1:p.Ser1152=
|
|
XM_011538082.2:c.3429C>T
|
XP_011536384.1:p.Ser1143=
|
|
XM_017019090.1:c.3456C>T
|
XP_016874579.1:p.Ser1152=
|
|
NM_015335.5:c.3459C>T
MANE Select
|
NP_056150.1:p.Ser1153=
|
|