ENST00000403665.7:c.1178C>G
MANE Select
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ENSP00000384957.2:p.Ala393Gly
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ENST00000264692.8:c.1016C>G
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ENSP00000264692.5:p.Ala339Gly
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ENST00000403665.6:c.1178C>G
|
ENSP00000384957.2:p.Ala393Gly
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NM_000128.3:c.1178C>G , LRG_583t1:c.1178C>G
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NP_000119.1:p.Ala393Gly
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XM_005262821.2:c.1181C>G
|
XP_005262878.1:p.Ala394Gly
|
|
XM_005262822.2:c.1181C>G
|
XP_005262879.1:p.Ala394Gly
|
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XM_005262823.2:c.911C>G
|
XP_005262880.1:p.Ala304Gly
|
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XM_005262824.1:c.1181C>G
|
XP_005262881.1:p.Ala394Gly
|
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XM_006714137.1:c.1133C>G
|
XP_006714200.1:p.Ala378Gly
|
|
XR_938706.1:n.1586C>G
|
|
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XR_938707.1:n.1586C>G
|
|
|
XM_005262821.4:c.1181C>G
|
XP_005262878.1:p.Ala394Gly
|
|
XM_005262822.4:c.1181C>G
|
XP_005262879.1:p.Ala394Gly
|
|
XM_005262823.4:c.911C>G
|
XP_005262880.1:p.Ala304Gly
|
|
XM_006714137.3:c.1133C>G
|
XP_006714200.1:p.Ala378Gly
|
|
XM_017007884.2:c.*2150C>G
|
XP_016863373.1:n.*2150C>G
|
|
XM_017007885.2:c.*46C>G
|
XP_016863374.1:n.*46C>G
|
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XR_001741172.2:n.1652C>G
|
|
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NM_000128.4:c.1178C>G
MANE Select
|
NP_000119.1:p.Ala393Gly
|
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