ENST00000368666.7:c.1002T>A
MANE Select
|
ENSP00000357655.4:p.Ser334=
|
|
ENST00000639360.1:c.903T>A
|
ENSP00000491774.1:p.Ser301=
|
|
ENST00000230529.9:c.1002T>A
|
ENSP00000230529.5:p.Ser334=
|
|
ENST00000361714.5:c.1002T>A
|
ENSP00000354734.2:p.Ser334=
|
|
ENST00000368663.4:c.*308T>A
|
ENSP00000357652.4:n.*308T>A
|
|
ENST00000368664.7:c.*406T>A
|
ENSP00000357653.3:n.*406T>A
|
|
ENST00000368666.6:c.1056T>A
|
ENSP00000357655.3:p.Ser352=
|
|
ENST00000409166.5:c.330T>A
|
ENSP00000386467.1:p.Ser110=
|
|
ENST00000454589.5:c.*406T>A
|
ENSP00000395928.1:n.*406T>A
|
|
ENST00000604763.5:c.1002T>A
|
ENSP00000473777.1:p.Ser334=
|
|
ENST00000613648.1:n.837T>A
|
|
|
ENST00000620524.3:n.933T>A
|
|
|
NM_003880.3:c.1002T>A
|
NP_003871.1:p.Ser334=
|
|
NM_198239.1:c.1056T>A
|
NP_937882.1:p.Ser352=
|
|
NR_125353.1:n.1256T>A
|
|
|
NR_125354.1:n.1176T>A
|
|
|
XM_011536220.1:c.1002T>A
|
XP_011534522.1:p.Ser334=
|
|
XM_011536221.1:c.*406T>A
|
XP_011534523.1:n.*406T>A
|
|
XM_011536223.1:c.420T>A
|
XP_011534525.1:p.Ser140=
|
|
XM_011536223.3:c.420T>A
|
XP_011534525.1:p.Ser140=
|
|
XR_001743705.1:n.1604T>A
|
|
|
NM_003880.4:c.1002T>A
|
NP_003871.1:p.Ser334=
|
|
NM_198239.2:c.1002T>A
MANE Select
|
NP_937882.2:p.Ser334=
|
|
NR_125353.2:n.1320T>A
|
|
|
NR_125354.3:n.1147T>A
|
|
|