ENST00000381588.9:c.1035T>A
MANE Select
|
ENSP00000371000.4:p.Gly345=
|
|
ENST00000346166.7:c.1035T>A
|
ENSP00000342121.3:p.Gly345=
|
|
ENST00000381570.7:c.1035T>A
|
ENSP00000370982.3:p.Gly345=
|
|
ENST00000381588.8:c.1035T>A
|
ENSP00000371000.4:p.Gly345=
|
|
ENST00000468480.5:n.768+627T>A
|
|
|
NM_005977.3:c.1035T>A
|
NP_005968.1:p.Gly345=
|
|
NM_183043.2:c.1035T>A
|
NP_898864.1:p.Gly345=
|
|
NM_183044.2:c.1035T>A
|
NP_898865.1:p.Gly345=
|
|
NM_183045.1:c.408+627T>A
|
NP_898866.1:n.408+627T>A
|
|
XM_005266485.1:c.1035T>A
|
XP_005266542.1:p.Gly345=
|
|
XM_005266486.1:c.1035T>A
|
XP_005266543.1:p.Gly345=
|
|
XM_011535177.1:c.1035T>A
|
XP_011533479.1:p.Gly345=
|
|
XM_011535178.1:c.408+627T>A
|
XP_011533480.1:n.408+627T>A
|
|
XM_005266485.3:c.1035T>A
|
XP_005266542.1:p.Gly345=
|
|
XM_005266486.2:c.1035T>A
|
XP_005266543.1:p.Gly345=
|
|
XM_011535177.3:c.1035T>A
|
XP_011533479.1:p.Gly345=
|
|
XM_011535178.2:c.408+627T>A
|
XP_011533480.1:n.408+627T>A
|
|
XM_017020685.2:c.409-78T>A
|
XP_016876174.1:n.409-78T>A
|
|
XM_017020686.1:c.409-78T>A
|
XP_016876175.1:n.409-78T>A
|
|
XM_017020687.1:c.409-78T>A
|
XP_016876176.1:n.409-78T>A
|
|
XM_024449390.1:c.1035T>A
|
XP_024305158.1:p.Gly345=
|
|
XM_024449391.1:c.409-78T>A
|
XP_024305159.1:n.409-78T>A
|
|
XM_024449392.1:c.409-78T>A
|
XP_024305160.1:n.409-78T>A
|
|
NM_005977.4:c.1035T>A
MANE Select
|
NP_005968.1:p.Gly345=
|
|
NM_183043.3:c.1035T>A
|
NP_898864.1:p.Gly345=
|
|
NM_183044.3:c.1035T>A
|
NP_898865.1:p.Gly345=
|
|