ENST00000403665.7:c.636C>A
MANE Select
|
ENSP00000384957.2:p.Asp212Glu
|
|
ENST00000264692.8:c.474C>A
|
ENSP00000264692.5:p.Asp158Glu
|
|
ENST00000403665.6:c.636C>A
|
ENSP00000384957.2:p.Asp212Glu
|
|
ENST00000452239.1:c.83C>A
|
|
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NM_000128.3:c.636C>A , LRG_583t1:c.636C>A
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NP_000119.1:p.Asp212Glu
|
|
XM_005262821.2:c.636C>A
|
XP_005262878.1:p.Asp212Glu
|
|
XM_005262822.2:c.636C>A
|
XP_005262879.1:p.Asp212Glu
|
|
XM_005262823.2:c.485+1996C>A
|
XP_005262880.1:n.485+1996C>A
|
|
XM_005262824.1:c.636C>A
|
XP_005262881.1:p.Asp212Glu
|
|
XM_006714137.1:c.636C>A
|
XP_006714200.1:p.Asp212Glu
|
|
XR_938706.1:n.988C>A
|
|
|
XR_938707.1:n.988C>A
|
|
|
XM_005262821.4:c.636C>A
|
XP_005262878.1:p.Asp212Glu
|
|
XM_005262822.4:c.636C>A
|
XP_005262879.1:p.Asp212Glu
|
|
XM_005262823.4:c.485+1996C>A
|
XP_005262880.1:n.485+1996C>A
|
|
XM_006714137.3:c.636C>A
|
XP_006714200.1:p.Asp212Glu
|
|
XM_017007884.2:c.636C>A
|
XP_016863373.1:p.Asp212Glu
|
|
XM_017007885.2:c.636C>A
|
XP_016863374.1:p.Asp212Glu
|
|
XM_017007886.2:c.636C>A
|
XP_016863375.1:p.Asp212Glu
|
|
XR_001741172.2:n.969C>A
|
|
|
NM_000128.4:c.636C>A
MANE Select
|
NP_000119.1:p.Asp212Glu
|
|