ENST00000346342.8:c.329G>A
MANE Select
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ENSP00000329546.4:p.Cys110Tyr
|
|
ENST00000346342.7:c.329G>A
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ENSP00000329546.3:p.Cys110Tyr
|
|
ENST00000375581.3:c.395G>A
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ENSP00000364731.3:p.Cys132Tyr
|
|
ENST00000444337.1:c.*137G>A
|
ENSP00000387669.1:n.*137G>A
|
|
ENST00000473085.1:n.276G>A
|
|
|
ENST00000479674.1:n.662G>A
|
|
|
ENST00000541084.5:c.143G>A
|
ENSP00000442051.2:p.Cys48Tyr
|
|
NM_000131.4:c.395G>A , LRG_554t1:c.395G>A
|
NP_000122.1:p.Cys132Tyr
|
|
NM_001267554.1:c.143G>A
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NP_001254483.1:p.Cys48Tyr
|
|
NM_019616.3:c.329G>A , LRG_554t2:c.329G>A
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NP_062562.1:p.Cys110Tyr
|
|
NR_051961.1:n.416G>A
|
|
|
XM_006719963.2:c.329G>A
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XP_006720026.1:p.Cys110Tyr
|
|
XM_011537474.1:c.329G>A
|
XP_011535776.1:p.Cys110Tyr
|
|
XM_011537475.1:c.143G>A
|
XP_011535777.1:p.Cys48Tyr
|
|
XM_011537477.1:c.290G>A
|
XP_011535779.1:p.Cys97Tyr
|
|
XM_006719963.3:c.374G>A
|
XP_006720026.2:p.Cys125Tyr
|
|
XM_011537474.2:c.374G>A
|
XP_011535776.2:p.Cys125Tyr
|
|
XM_011537475.2:c.188G>A
|
XP_011535777.2:p.Cys63Tyr
|
|
NM_019616.4:c.329G>A
MANE Select
|
NP_062562.1:p.Cys110Tyr
|
|
NR_051961.2:n.413G>A
|
|
|
NM_001267554.2:c.143G>A
|
NP_001254483.1:p.Cys48Tyr
|
|