ENST00000310123.8:c.759C>T
MANE Select
|
ENSP00000312273.3:p.Ser253=
|
|
ENST00000310123.7:c.759C>T
|
ENSP00000312273.3:p.Ser253=
|
|
ENST00000392225.7:c.759C>T
|
ENSP00000376059.3:p.Ser253=
|
|
ENST00000493050.5:n.818C>T
|
|
|
ENST00000587780.5:c.494C>T
|
|
|
ENST00000591840.5:n.420-2021C>T
|
|
|
ENST00000593248.5:n.890C>T
|
|
|
NM_139284.2:c.759C>T
|
NP_644813.1:p.Ser253=
|
|
XM_011526594.1:c.759C>T
|
XP_011524896.1:p.Ser253=
|
|
XM_011526595.1:c.243C>T
|
XP_011524897.1:p.Ser81=
|
|
XM_011526595.2:c.243C>T
|
XP_011524897.1:p.Ser81=
|
|
XM_017026428.1:c.243C>T
|
XP_016881917.1:p.Ser81=
|
|
XM_017026429.1:c.243C>T
|
XP_016881918.1:p.Ser81=
|
|
XM_017026430.2:c.243C>T
|
XP_016881919.1:p.Ser81=
|
|
NM_139284.3:c.759C>T
MANE Select
|
NP_644813.1:p.Ser253=
|
|