ENST00000262407.6:c.722G=
MANE Select
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ENSP00000262407.5:p.Gly241=
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ENST00000648408.1:c.153G=
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|
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ENST00000262407.5:c.722G=
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ENSP00000262407.5:p.Gly241=
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ENST00000589645.5:n.173G=
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|
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ENST00000591990.5:n.84G=
|
|
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ENST00000592075.5:n.91G=
|
|
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ENST00000592226.5:n.39+139G=
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|
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ENST00000592253.5:n.230G=
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|
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ENST00000592944.1:n.404G=
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|
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NM_000419.3:c.722G= , LRG_479t1:c.722G=
|
NP_000410.2:p.Gly241=
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XM_011524749.1:c.722G=
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XP_011523051.1:p.Gly241=
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XM_011524750.1:c.722G=
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XP_011523052.1:p.Gly241=
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|
NM_000419.4:c.722G=
|
NP_000410.2:p.Gly241=
|
|
NM_000419.5:c.722G=
MANE Select
|
NP_000410.2:p.Gly241=
|
|