ENST00000477226.6:n.322C>T
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|
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ENST00000683013.1:n.236C>T
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|
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ENST00000373960.4:c.848C>T
MANE Select
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ENSP00000363071.3:p.Thr283Ile
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ENST00000373960.3:c.848C>T
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ENSP00000363071.3:p.Thr283Ile
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ENST00000477226.5:n.320C>T
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|
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ENST00000492726.1:n.243C>T
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NM_001927.3:c.848C>T , LRG_380t1:c.848C>T
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NP_001918.3:p.Thr283Ile
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|
NM_001927.4:c.848C>T
MANE Select
|
NP_001918.3:p.Thr283Ile
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NM_001382708.1:c.845C>T
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NP_001369637.1:p.Thr282Ile
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NM_001382709.1:c.735+261C>T
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NP_001369638.1:n.735+261C>T
|
|
NM_001382710.1:c.848C>T
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NP_001369639.1:p.Thr283Ile
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NM_001382711.1:c.848C>T
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NP_001369640.1:p.Thr283Ile
|
|
NM_001382712.1:c.848C>T
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NP_001369641.1:p.Thr283Ile
|
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NM_001382713.1:c.578C>T
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NP_001369642.1:p.Thr193Ile
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