ENST00000673913.2:c.1553A>C
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ENSP00000501161.2:p.Glu518Ala
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ENST00000710286.1:c.1910A>C
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ENSP00000518176.1:p.Glu637Ala
|
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ENST00000673903.1:c.1178A>C
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ENSP00000501257.1:p.Glu393Ala
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ENST00000673913.1:c.293A>C
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ENSP00000501161.1:p.Glu98Ala
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ENST00000302118.5:c.1553A>C
MANE Select
|
ENSP00000303208.5:p.Glu518Ala
|
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ENST00000490692.1:n.2227+888A>C
|
|
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NM_174936.3:c.1553A>C , LRG_275t1:c.1553A>C
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NP_777596.2:p.Glu518Ala
|
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NR_110451.1:n.1160A>C
|
|
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XM_011541193.1:c.674A>C
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XP_011539495.1:p.Glu225Ala
|
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NM_174936.4:c.1553A>C
MANE Select
|
NP_777596.2:p.Glu518Ala
|
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NR_110451.2:n.1160A>C
|
|
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