ENST00000346342.8:c.1129T=
MANE Select
|
ENSP00000329546.4:p.Ser377=
|
|
ENST00000346342.7:c.1129T=
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ENSP00000329546.3:p.Ser377=
|
|
ENST00000375581.3:c.1195T=
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ENSP00000364731.3:p.Ser399=
|
|
ENST00000541084.5:c.943T=
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ENSP00000442051.2:p.Ser315=
|
|
NM_000131.4:c.1195T= , LRG_554t1:c.1195T=
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NP_000122.1:p.Ser399=
|
|
NM_001267554.1:c.943T=
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NP_001254483.1:p.Ser315=
|
|
NM_019616.3:c.1129T= , LRG_554t2:c.1129T=
|
NP_062562.1:p.Ser377=
|
|
NR_051961.1:n.1216T=
|
|
|
XM_006719963.2:c.988T=
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XP_006720026.1:p.Ser330=
|
|
XM_011537474.1:c.1237T=
|
XP_011535776.1:p.Ser413=
|
|
XM_011537475.1:c.1051T=
|
XP_011535777.1:p.Ser351=
|
|
XM_011537476.1:c.889T=
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XP_011535778.1:p.Ser297=
|
|
XM_011537477.1:c.1198T=
|
XP_011535779.1:p.Ser400=
|
|
XM_006719963.3:c.1033T=
|
XP_006720026.2:p.Ser345=
|
|
XM_011537474.2:c.1282T=
|
XP_011535776.2:p.Ser428=
|
|
XM_011537475.2:c.1096T=
|
XP_011535777.2:p.Ser366=
|
|
XM_011537476.2:c.889T=
|
XP_011535778.1:p.Ser297=
|
|
NM_019616.4:c.1129T=
MANE Select
|
NP_062562.1:p.Ser377=
|
|
NR_051961.2:n.1213T=
|
|
|
NM_001267554.2:c.943T=
|
NP_001254483.1:p.Ser315=
|
|