ENST00000403665.7:c.1433G>A
MANE Select
|
ENSP00000384957.2:p.Gly478Glu
|
|
ENST00000264691.4:c.129G>A
|
|
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ENST00000264692.8:c.1271G>A
|
ENSP00000264692.5:p.Gly424Glu
|
|
ENST00000403665.6:c.1433G>A
|
ENSP00000384957.2:p.Gly478Glu
|
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NM_000128.3:c.1433G>A , LRG_583t1:c.1433G>A
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NP_000119.1:p.Gly478Glu
|
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XM_005262821.2:c.1436G>A
|
XP_005262878.1:p.Gly479Glu
|
|
XM_005262822.2:c.1436G>A
|
XP_005262879.1:p.Gly479Glu
|
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XM_005262823.2:c.1166G>A
|
XP_005262880.1:p.Gly389Glu
|
|
XM_005262824.1:c.1436G>A
|
XP_005262881.1:p.Gly479Glu
|
|
XM_006714137.1:c.1388G>A
|
XP_006714200.1:p.Gly463Glu
|
|
XR_938706.1:n.1841G>A
|
|
|
XR_938707.1:n.1841G>A
|
|
|
XM_005262821.4:c.1436G>A
|
XP_005262878.1:p.Gly479Glu
|
|
XM_005262822.4:c.1436G>A
|
XP_005262879.1:p.Gly479Glu
|
|
XM_005262823.4:c.1166G>A
|
XP_005262880.1:p.Gly389Glu
|
|
XM_006714137.3:c.1388G>A
|
XP_006714200.1:p.Gly463Glu
|
|
XR_001741172.2:n.1907G>A
|
|
|
NM_000128.4:c.1433G>A
MANE Select
|
NP_000119.1:p.Gly478Glu
|
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