ENST00000673913.2:c.*175A>C
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ENSP00000501161.2:n.*175A>C
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|
ENST00000710286.1:c.2192A>C
|
ENSP00000518176.1:p.Glu731Ala
|
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ENST00000673903.1:c.1460A>C
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ENSP00000501257.1:p.Glu487Ala
|
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ENST00000673913.1:c.685A>C
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ENSP00000501161.1:n.685A>C
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ENST00000302118.5:c.1835A>C
MANE Select
|
ENSP00000303208.5:p.Glu612Ala
|
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ENST00000490692.1:n.2381A>C
|
|
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NM_174936.3:c.1835A>C , LRG_275t1:c.1835A>C
|
NP_777596.2:p.Glu612Ala
|
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NR_110451.1:n.1442A>C
|
|
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XM_011541193.1:c.956A>C
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XP_011539495.1:p.Glu319Ala
|
|
NM_174936.4:c.1835A>C
MANE Select
|
NP_777596.2:p.Glu612Ala
|
|
NR_110451.2:n.1442A>C
|
|
|