ENST00000403665.7:c.1190G>T
MANE Select
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ENSP00000384957.2:p.Gly397Val
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ENST00000264692.8:c.1028G>T
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ENSP00000264692.5:p.Gly343Val
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ENST00000403665.6:c.1190G>T
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ENSP00000384957.2:p.Gly397Val
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NM_000128.3:c.1190G>T , LRG_583t1:c.1190G>T
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NP_000119.1:p.Gly397Val
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XM_005262821.2:c.1193G>T
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XP_005262878.1:p.Gly398Val
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XM_005262822.2:c.1193G>T
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XP_005262879.1:p.Gly398Val
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XM_005262823.2:c.923G>T
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XP_005262880.1:p.Gly308Val
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XM_005262824.1:c.1193G>T
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XP_005262881.1:p.Gly398Val
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XM_006714137.1:c.1145G>T
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XP_006714200.1:p.Gly382Val
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XR_938706.1:n.1598G>T
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XR_938707.1:n.1598G>T
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XM_005262821.4:c.1193G>T
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XP_005262878.1:p.Gly398Val
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XM_005262822.4:c.1193G>T
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XP_005262879.1:p.Gly398Val
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XM_005262823.4:c.923G>T
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XP_005262880.1:p.Gly308Val
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XM_006714137.3:c.1145G>T
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XP_006714200.1:p.Gly382Val
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XM_017007884.2:c.*2162G>T
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XP_016863373.1:n.*2162G>T
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XM_017007885.2:c.*58G>T
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XP_016863374.1:n.*58G>T
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XR_001741172.2:n.1664G>T
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NM_000128.4:c.1190G>T
MANE Select
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NP_000119.1:p.Gly397Val
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