ENST00000252288.8:c.477G>T
MANE Select
|
ENSP00000252288.1:p.Leu159=
|
|
ENST00000447102.8:c.477G>T
|
ENSP00000403536.2:p.Leu159=
|
|
ENST00000591788.3:c.160G>T
|
|
|
ENST00000640164.1:n.310G>T
|
|
|
ENST00000640762.1:c.408G>T
|
ENSP00000492031.1:p.Leu136=
|
|
ENST00000252288.6:c.477G>T
|
ENSP00000252288.1:p.Leu159=
|
|
ENST00000447102.7:c.477G>T
|
ENSP00000403536.2:p.Leu159=
|
|
ENST00000591788.2:c.162G>T
|
ENSP00000466341.2:p.Leu54=
|
|
NM_000156.5:c.477G>T
|
NP_000147.1:p.Leu159=
|
|
NM_138924.2:c.477G>T
|
NP_620279.1:p.Leu159=
|
|
NM_000156.6:c.477G>T
MANE Select
|
NP_000147.1:p.Leu159=
|
|
NM_138924.3:c.477G>T
|
NP_620279.1:p.Leu159=
|
|