ENST00000477226.6:n.371+33G>T
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|
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ENST00000683013.1:n.285+33G>T
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|
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ENST00000373960.4:c.897+33G>T
MANE Select
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ENSP00000363071.3:n.897+33G>T
|
|
ENST00000373960.3:c.897+33G>T
|
ENSP00000363071.3:n.897+33G>T
|
|
ENST00000477226.5:n.369+33G>T
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|
|
ENST00000492726.1:n.292+33G>T
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|
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NM_001927.3:c.897+33G>T , LRG_380t1:c.897+33G>T
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NP_001918.3:n.897+33G>T
|
|
NM_001927.4:c.897+33G>T
MANE Select
|
NP_001918.3:n.897+33G>T
|
|
NM_001382708.1:c.894+33G>T
|
NP_001369637.1:n.894+33G>T
|
|
NM_001382709.1:c.735+343G>T
|
NP_001369638.1:n.735+343G>T
|
|
NM_001382710.1:c.897+33G>T
|
NP_001369639.1:n.897+33G>T
|
|
NM_001382711.1:c.897+33G>T
|
NP_001369640.1:n.897+33G>T
|
|
NM_001382712.1:c.897+33G>T
|
NP_001369641.1:n.897+33G>T
|
|
NM_001382713.1:c.627+33G>T
|
NP_001369642.1:n.627+33G>T
|
|