ENST00000398603.6:c.347C=
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ENSP00000381604.1:p.Ala116=
|
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ENST00000398606.10:c.455C=
MANE Select
|
ENSP00000381607.3:p.Ala152=
|
|
ENST00000646888.1:c.*171C=
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ENSP00000494477.1:n.*171C=
|
|
ENST00000398603.5:c.347C=
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ENSP00000381604.1:p.Ala116=
|
|
ENST00000398606.7:c.455C=
|
ENSP00000381607.3:p.Ala152=
|
|
ENST00000467591.1:n.566C=
|
|
|
ENST00000494593.1:n.1427C=
|
|
|
ENST00000495996.1:c.181C=
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ENSP00000484686.1:p.Leu61=
|
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ENST00000498765.5:c.518C=
|
|
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NM_000852.3:c.455C= , LRG_723t1:c.455C=
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NP_000843.1:p.Ala152=
|
|
NM_000852.4:c.455C=
MANE Select
|
NP_000843.1:p.Ala152=
|
|