ENST00000346342.8:c.1301G=
MANE Select
|
ENSP00000329546.4:p.Arg434=
|
|
ENST00000346342.7:c.1301G=
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ENSP00000329546.3:p.Arg434=
|
|
ENST00000375581.3:c.1367G=
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ENSP00000364731.3:p.Arg456=
|
|
ENST00000541084.5:c.1115G=
|
ENSP00000442051.2:p.Arg372=
|
|
NM_000131.4:c.1367G= , LRG_554t1:c.1367G=
|
NP_000122.1:p.Arg456=
|
|
NM_001267554.1:c.1115G=
|
NP_001254483.1:p.Arg372=
|
|
NM_019616.3:c.1301G= , LRG_554t2:c.1301G=
|
NP_062562.1:p.Arg434=
|
|
NR_051961.1:n.1388G=
|
|
|
XM_006719963.2:c.1160G=
|
XP_006720026.1:p.Arg387=
|
|
XM_011537474.1:c.1409G=
|
XP_011535776.1:p.Arg470=
|
|
XM_011537475.1:c.1223G=
|
XP_011535777.1:p.Arg408=
|
|
XM_011537476.1:c.1061G=
|
XP_011535778.1:p.Arg354=
|
|
XM_011537477.1:c.1370G=
|
XP_011535779.1:p.Arg457=
|
|
XM_006719963.3:c.1205G=
|
XP_006720026.2:p.Arg402=
|
|
XM_011537474.2:c.1454G=
|
XP_011535776.2:p.Arg485=
|
|
XM_011537475.2:c.1268G=
|
XP_011535777.2:p.Arg423=
|
|
XM_011537476.2:c.1061G=
|
XP_011535778.1:p.Arg354=
|
|
NM_019616.4:c.1301G=
MANE Select
|
NP_062562.1:p.Arg434=
|
|
NR_051961.2:n.1385G=
|
|
|
NM_001267554.2:c.1115G=
|
NP_001254483.1:p.Arg372=
|
|