ENST00000256084.8:c.3045T>A
MANE Select
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ENSP00000256084.7:p.Gly1015=
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ENST00000256084.7:c.3045T>A
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ENSP00000256084.7:p.Gly1015=
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ENST00000359874.7:c.3135T>A
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ENSP00000352936.3:p.Gly1045=
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NM_001127698.1:c.3135T>A
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NP_001121170.1:p.Gly1045=
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NM_006846.3:c.3045T>A , LRG_110t1:c.3045T>A
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NP_006837.2:p.Gly1015=
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XM_011537550.1:c.3078T>A
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XP_011535852.1:p.Gly1026=
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XM_011537551.1:c.3051T>A
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XP_011535853.1:p.Gly1017=
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XM_011537551.2:c.3051T>A
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XP_011535853.1:p.Gly1017=
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NM_001127698.2:c.3135T>A
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NP_001121170.1:p.Gly1045=
|
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NM_006846.4:c.3045T>A
MANE Select
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NP_006837.2:p.Gly1015=
|
|