ENST00000403665.7:c.1136-93T=
MANE Select
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ENSP00000384957.2:n.1136-93T=
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ENST00000264692.8:c.974-93T=
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ENSP00000264692.5:n.974-93T=
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ENST00000403665.6:c.1136-93T=
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ENSP00000384957.2:n.1136-93T=
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NM_000128.3:c.1136-93T= , LRG_583t1:c.1136-93T=
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NP_000119.1:n.1136-93T=
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XM_005262821.2:c.1139-93T=
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XP_005262878.1:n.1139-93T=
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XM_005262822.2:c.1139-93T=
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XP_005262879.1:n.1139-93T=
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XM_005262823.2:c.869-93T=
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XP_005262880.1:n.869-93T=
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XM_005262824.1:c.1139-93T=
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XP_005262881.1:n.1139-93T=
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XM_006714137.1:c.1091-93T=
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XP_006714200.1:n.1091-93T=
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XR_938706.1:n.1544-93T=
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XR_938707.1:n.1544-93T=
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XM_005262821.4:c.1139-93T=
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XP_005262878.1:n.1139-93T=
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XM_005262822.4:c.1139-93T=
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XP_005262879.1:n.1139-93T=
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XM_005262823.4:c.869-93T=
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XP_005262880.1:n.869-93T=
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XM_006714137.3:c.1091-93T=
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XP_006714200.1:n.1091-93T=
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XM_017007884.2:c.*2015T=
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XP_016863373.1:n.*2015T=
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XM_017007885.2:c.*4-93T=
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XP_016863374.1:n.*4-93T=
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XR_001741172.2:n.1610-93T=
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NM_000128.4:c.1136-93T=
MANE Select
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NP_000119.1:n.1136-93T=
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