ENST00000477226.6:n.313A=
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|
|
ENST00000683013.1:n.227A=
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|
|
ENST00000373960.4:c.839A=
MANE Select
|
ENSP00000363071.3:p.Gln280=
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|
ENST00000373960.3:c.839A=
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ENSP00000363071.3:p.Gln280=
|
|
ENST00000477226.5:n.311A=
|
|
|
ENST00000492726.1:n.234A=
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|
|
NM_001927.3:c.839A= , LRG_380t1:c.839A=
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NP_001918.3:p.Gln280=
|
|
NM_001927.4:c.839A=
MANE Select
|
NP_001918.3:p.Gln280=
|
|
NM_001382708.1:c.836A=
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NP_001369637.1:p.Gln279=
|
|
NM_001382709.1:c.735+252A=
|
NP_001369638.1:n.735+252A=
|
|
NM_001382710.1:c.839A=
|
NP_001369639.1:p.Gln280=
|
|
NM_001382711.1:c.839A=
|
NP_001369640.1:p.Gln280=
|
|
NM_001382712.1:c.839A=
|
NP_001369641.1:p.Gln280=
|
|
NM_001382713.1:c.569A=
|
NP_001369642.1:p.Gln190=
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|