ENST00000496887.7:c.643G=
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ENSP00000434560.2:p.Ala215=
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ENST00000646564.2:c.478-10466G=
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ENSP00000495806.2:n.478-10466G=
|
|
ENST00000155840.12:c.904G=
MANE Select
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ENSP00000155840.2:p.Ala302=
|
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ENST00000335475.6:c.523G=
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ENSP00000334497.5:p.Ala175=
|
|
ENST00000646564.1:c.124-10466G=
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ENSP00000495806.1:n.124-10466G=
|
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ENST00000155840.9:c.904G=
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ENSP00000155840.2:p.Ala302=
|
|
ENST00000335475.5:c.523G=
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ENSP00000334497.5:p.Ala175=
|
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NM_000218.2:c.904G= , LRG_287t1:c.904G=
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NP_000209.2:p.Ala302=
|
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NM_181798.1:c.523G= , LRG_287t2:c.523G=
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NP_861463.1:p.Ala175=
|
|
NM_000218.3:c.904G=
MANE Select
|
NP_000209.2:p.Ala302=
|
|