ENST00000403665.7:c.1289C>G
MANE Select
|
ENSP00000384957.2:p.Ala430Gly
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ENST00000264692.8:c.1127C>G
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ENSP00000264692.5:p.Ala376Gly
|
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ENST00000403665.6:c.1289C>G
|
ENSP00000384957.2:p.Ala430Gly
|
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NM_000128.3:c.1289C>G , LRG_583t1:c.1289C>G
|
NP_000119.1:p.Ala430Gly
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XM_005262821.2:c.1292C>G
|
XP_005262878.1:p.Ala431Gly
|
|
XM_005262822.2:c.1292C>G
|
XP_005262879.1:p.Ala431Gly
|
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XM_005262823.2:c.1022C>G
|
XP_005262880.1:p.Ala341Gly
|
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XM_005262824.1:c.1292C>G
|
XP_005262881.1:p.Ala431Gly
|
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XM_006714137.1:c.1244C>G
|
XP_006714200.1:p.Ala415Gly
|
|
XR_938706.1:n.1697C>G
|
|
|
XR_938707.1:n.1697C>G
|
|
|
XM_005262821.4:c.1292C>G
|
XP_005262878.1:p.Ala431Gly
|
|
XM_005262822.4:c.1292C>G
|
XP_005262879.1:p.Ala431Gly
|
|
XM_005262823.4:c.1022C>G
|
XP_005262880.1:p.Ala341Gly
|
|
XM_006714137.3:c.1244C>G
|
XP_006714200.1:p.Ala415Gly
|
|
XR_001741172.2:n.1763C>G
|
|
|
NM_000128.4:c.1289C>G
MANE Select
|
NP_000119.1:p.Ala430Gly
|
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