ENST00000673913.2:c.1631C=
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ENSP00000501161.2:p.Ala544=
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ENST00000710286.1:c.1988C=
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ENSP00000518176.1:p.Ala663=
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ENST00000673903.1:c.1256C=
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ENSP00000501257.1:p.Ala419=
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ENST00000673913.1:c.371C=
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ENSP00000501161.1:p.Ala124=
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ENST00000302118.5:c.1631C=
MANE Select
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ENSP00000303208.5:p.Ala544=
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ENST00000490692.1:n.2227+966C=
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NM_174936.3:c.1631C= , LRG_275t1:c.1631C=
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NP_777596.2:p.Ala544=
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NR_110451.1:n.1238C=
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XM_011541193.1:c.752C=
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XP_011539495.1:p.Ala251=
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NM_174936.4:c.1631C=
MANE Select
|
NP_777596.2:p.Ala544=
|
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NR_110451.2:n.1238C=
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