ENST00000222214.10:c.868C>T
MANE Select
|
ENSP00000222214.4:p.Leu290=
|
|
ENST00000222214.9:c.868C>T
|
ENSP00000222214.4:p.Leu290=
|
|
ENST00000421816.6:n.846C>T
|
|
|
ENST00000585420.5:n.1198C>T
|
|
|
ENST00000590530.5:c.*308C>T
|
ENSP00000468452.1:n.*308C>T
|
|
ENST00000591043.1:n.904C>T
|
|
|
ENST00000591470.5:c.868C>T
|
ENSP00000466845.1:p.Leu290=
|
|
NM_000159.3:c.868C>T
|
NP_000150.1:p.Leu290=
|
|
NM_013976.3:c.868C>T
|
NP_039663.1:p.Leu290=
|
|
NR_102316.1:n.1031C>T
|
|
|
NR_102317.1:n.1249C>T
|
|
|
XM_006722721.2:c.868C>T
|
XP_006722784.1:p.Leu290=
|
|
XM_011527899.1:c.868C>T
|
XP_011526201.1:p.Leu290=
|
|
XM_011527900.1:c.868C>T
|
XP_011526202.1:p.Leu290=
|
|
XM_011527899.2:c.868C>T
|
XP_011526201.1:p.Leu290=
|
|
XM_011527900.2:c.868C>T
|
XP_011526202.1:p.Leu290=
|
|
XM_017026580.1:c.868C>T
|
XP_016882069.1:p.Leu290=
|
|
NM_000159.4:c.868C>T
MANE Select
|
NP_000150.1:p.Leu290=
|
|
NM_013976.4:c.868C>T
|
NP_039663.1:p.Leu290=
|
|
NM_013976.5:c.868C>T
|
NP_039663.1:p.Leu290=
|
|