ENST00000368666.7:c.983A>T
MANE Select
|
ENSP00000357655.4:p.Lys328Met
|
|
ENST00000639360.1:c.884A>T
|
ENSP00000491774.1:p.Lys295Met
|
|
ENST00000230529.9:c.983A>T
|
ENSP00000230529.5:p.Lys328Met
|
|
ENST00000361714.5:c.983A>T
|
ENSP00000354734.2:p.Lys328Met
|
|
ENST00000368663.4:c.*289A>T
|
ENSP00000357652.4:n.*289A>T
|
|
ENST00000368664.7:c.*387A>T
|
ENSP00000357653.3:n.*387A>T
|
|
ENST00000368666.6:c.1037A>T
|
ENSP00000357655.3:p.Lys346Met
|
|
ENST00000409166.5:c.311A>T
|
ENSP00000386467.1:p.Lys104Met
|
|
ENST00000454589.5:c.*387A>T
|
ENSP00000395928.1:n.*387A>T
|
|
ENST00000604763.5:c.983A>T
|
ENSP00000473777.1:p.Lys328Met
|
|
ENST00000613648.1:n.818A>T
|
|
|
ENST00000620524.3:n.914A>T
|
|
|
NM_003880.3:c.983A>T
|
NP_003871.1:p.Lys328Met
|
|
NM_198239.1:c.1037A>T
|
NP_937882.1:p.Lys346Met
|
|
NR_125353.1:n.1237A>T
|
|
|
NR_125354.1:n.1157A>T
|
|
|
XM_011536220.1:c.983A>T
|
XP_011534522.1:p.Lys328Met
|
|
XM_011536221.1:c.*387A>T
|
XP_011534523.1:n.*387A>T
|
|
XM_011536223.1:c.401A>T
|
XP_011534525.1:p.Lys134Met
|
|
XM_011536223.3:c.401A>T
|
XP_011534525.1:p.Lys134Met
|
|
XR_001743705.1:n.1585A>T
|
|
|
NM_003880.4:c.983A>T
|
NP_003871.1:p.Lys328Met
|
|
NM_198239.2:c.983A>T
MANE Select
|
NP_937882.2:p.Lys328Met
|
|
NR_125353.2:n.1301A>T
|
|
|
NR_125354.3:n.1128A>T
|
|
|