ENST00000333188.10:c.760C>T
MANE Select
|
ENSP00000329419.4:p.Arg254Cys
|
|
ENST00000503326.6:c.760C>T
|
ENSP00000426682.2:p.Arg254Cys
|
|
ENST00000507777.6:c.673C>T
|
ENSP00000422295.1:p.Arg225Cys
|
|
ENST00000510181.6:c.526C>T
|
ENSP00000502846.1:p.Arg176Cys
|
|
ENST00000512242.6:c.673C>T
|
ENSP00000427185.2:p.Arg225Cys
|
|
ENST00000512309.2:c.760C>T
|
ENSP00000422917.2:p.Arg254Cys
|
|
ENST00000514508.2:c.673C>T
|
ENSP00000422469.2:p.Arg225Cys
|
|
ENST00000677073.1:c.*722C>T
|
ENSP00000504033.1:n.*722C>T
|
|
ENST00000677309.1:c.752-388C>T
|
ENSP00000503548.1:n.752-388C>T
|
|
ENST00000677601.1:c.785C>T
|
ENSP00000503393.1:p.Thr262Met
|
|
ENST00000677882.1:n.1547C>T
|
|
|
ENST00000333188.9:c.760C>T
|
ENSP00000329419.4:p.Arg254Cys
|
|
ENST00000507777.5:c.673C>T
|
ENSP00000422295.1:p.Arg225Cys
|
|
NM_004766.2:c.760C>T
|
NP_004757.1:p.Arg254Cys
|
|
NR_023350.1:n.969C>T
|
|
|
XM_011513317.1:c.133-388C>T
|
XP_011511619.1:n.133-388C>T
|
|
XM_017007513.1:c.133-388C>T
|
XP_016863002.1:n.133-388C>T
|
|
XM_024453831.1:c.133-388C>T
|
XP_024309599.1:n.133-388C>T
|
|
NM_004766.3:c.760C>T
MANE Select
|
NP_004757.1:p.Arg254Cys
|
|