ENST00000346342.8:c.1293A>C
MANE Select
|
ENSP00000329546.4:p.Ser431=
|
|
ENST00000346342.7:c.1293A>C
|
ENSP00000329546.3:p.Ser431=
|
|
ENST00000375581.3:c.1359A>C
|
ENSP00000364731.3:p.Ser453=
|
|
ENST00000541084.5:c.1107A>C
|
ENSP00000442051.2:p.Ser369=
|
|
NM_000131.4:c.1359A>C , LRG_554t1:c.1359A>C
|
NP_000122.1:p.Ser453=
|
|
NM_001267554.1:c.1107A>C
|
NP_001254483.1:p.Ser369=
|
|
NM_019616.3:c.1293A>C , LRG_554t2:c.1293A>C
|
NP_062562.1:p.Ser431=
|
|
NR_051961.1:n.1380A>C
|
|
|
XM_006719963.2:c.1152A>C
|
XP_006720026.1:p.Ser384=
|
|
XM_011537474.1:c.1401A>C
|
XP_011535776.1:p.Ser467=
|
|
XM_011537475.1:c.1215A>C
|
XP_011535777.1:p.Ser405=
|
|
XM_011537476.1:c.1053A>C
|
XP_011535778.1:p.Ser351=
|
|
XM_011537477.1:c.1362A>C
|
XP_011535779.1:p.Ser454=
|
|
XM_006719963.3:c.1197A>C
|
XP_006720026.2:p.Ser399=
|
|
XM_011537474.2:c.1446A>C
|
XP_011535776.2:p.Ser482=
|
|
XM_011537475.2:c.1260A>C
|
XP_011535777.2:p.Ser420=
|
|
XM_011537476.2:c.1053A>C
|
XP_011535778.1:p.Ser351=
|
|
NM_019616.4:c.1293A>C
MANE Select
|
NP_062562.1:p.Ser431=
|
|
NR_051961.2:n.1377A>C
|
|
|
NM_001267554.2:c.1107A>C
|
NP_001254483.1:p.Ser369=
|
|