ENST00000477226.6:n.692G>A
|
|
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ENST00000683013.1:n.606G>A
|
|
|
ENST00000373960.4:c.1218G>A
MANE Select
|
ENSP00000363071.3:p.Arg406=
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|
ENST00000373960.3:c.1218G>A
|
ENSP00000363071.3:p.Arg406=
|
|
ENST00000477226.5:n.690G>A
|
|
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ENST00000492726.1:n.613G>A
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|
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NM_001927.3:c.1218G>A , LRG_380t1:c.1218G>A
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NP_001918.3:p.Arg406=
|
|
NM_001927.4:c.1218G>A
MANE Select
|
NP_001918.3:p.Arg406=
|
|
NM_001382708.1:c.1215G>A
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NP_001369637.1:p.Arg405=
|
|
NM_001382709.1:c.786G>A
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NP_001369638.1:p.Arg262=
|
|
NM_001382710.1:c.1149G>A
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NP_001369639.1:p.Arg383=
|
|
NM_001382711.1:c.1197G>A
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NP_001369640.1:p.Arg399=
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|
NM_001382712.1:c.1218G>A
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NP_001369641.1:p.Arg406=
|
|
NM_001382713.1:c.948G>A
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NP_001369642.1:p.Arg316=
|
|