ENST00000300026.4:c.336C>T
MANE Select
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ENSP00000300026.4:p.Gly112=
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ENST00000561048.2:n.369C>T
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ENST00000680158.1:c.336C>T
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ENSP00000504873.1:p.Gly112=
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ENST00000680343.1:n.290C>T
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ENST00000681397.1:c.336C>T
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ENSP00000506584.1:p.Gly112=
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ENST00000681658.1:c.231C>T
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ENSP00000505431.1:p.Gly77=
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ENST00000300026.3:c.336C>T
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ENSP00000300026.3:p.Gly112=
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ENST00000558492.1:n.242C>T
|
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ENST00000561048.1:n.371C>T
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NM_000942.4:c.336C>T , LRG_10t1:c.336C>T
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NP_000933.1:p.Gly112=
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NM_000942.5:c.336C>T
MANE Select
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NP_000933.1:p.Gly112=
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