ENST00000403665.7:c.1424C>A
MANE Select
|
ENSP00000384957.2:p.Ala475Glu
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ENST00000264691.4:c.120C>A
|
|
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ENST00000264692.8:c.1262C>A
|
ENSP00000264692.5:p.Ala421Glu
|
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ENST00000403665.6:c.1424C>A
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ENSP00000384957.2:p.Ala475Glu
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NM_000128.3:c.1424C>A , LRG_583t1:c.1424C>A
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NP_000119.1:p.Ala475Glu
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XM_005262821.2:c.1427C>A
|
XP_005262878.1:p.Ala476Glu
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XM_005262822.2:c.1427C>A
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XP_005262879.1:p.Ala476Glu
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XM_005262823.2:c.1157C>A
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XP_005262880.1:p.Ala386Glu
|
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XM_005262824.1:c.1427C>A
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XP_005262881.1:p.Ala476Glu
|
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XM_006714137.1:c.1379C>A
|
XP_006714200.1:p.Ala460Glu
|
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XR_938706.1:n.1832C>A
|
|
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XR_938707.1:n.1832C>A
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|
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XM_005262821.4:c.1427C>A
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XP_005262878.1:p.Ala476Glu
|
|
XM_005262822.4:c.1427C>A
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XP_005262879.1:p.Ala476Glu
|
|
XM_005262823.4:c.1157C>A
|
XP_005262880.1:p.Ala386Glu
|
|
XM_006714137.3:c.1379C>A
|
XP_006714200.1:p.Ala460Glu
|
|
XR_001741172.2:n.1898C>A
|
|
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NM_000128.4:c.1424C>A
MANE Select
|
NP_000119.1:p.Ala475Glu
|
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