ENST00000403665.7:c.1265G>C
MANE Select
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ENSP00000384957.2:p.Gly422Ala
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ENST00000264692.8:c.1103G>C
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ENSP00000264692.5:p.Gly368Ala
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ENST00000403665.6:c.1265G>C
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ENSP00000384957.2:p.Gly422Ala
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NM_000128.3:c.1265G>C , LRG_583t1:c.1265G>C
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NP_000119.1:p.Gly422Ala
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XM_005262821.2:c.1268G>C
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XP_005262878.1:p.Gly423Ala
|
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XM_005262822.2:c.1268G>C
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XP_005262879.1:p.Gly423Ala
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XM_005262823.2:c.998G>C
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XP_005262880.1:p.Gly333Ala
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XM_005262824.1:c.1268G>C
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XP_005262881.1:p.Gly423Ala
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XM_006714137.1:c.1220G>C
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XP_006714200.1:p.Gly407Ala
|
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XR_938706.1:n.1673G>C
|
|
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XR_938707.1:n.1673G>C
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|
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XM_005262821.4:c.1268G>C
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XP_005262878.1:p.Gly423Ala
|
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XM_005262822.4:c.1268G>C
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XP_005262879.1:p.Gly423Ala
|
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XM_005262823.4:c.998G>C
|
XP_005262880.1:p.Gly333Ala
|
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XM_006714137.3:c.1220G>C
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XP_006714200.1:p.Gly407Ala
|
|
XR_001741172.2:n.1739G>C
|
|
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NM_000128.4:c.1265G>C
MANE Select
|
NP_000119.1:p.Gly422Ala
|
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