ENST00000673913.2:c.1556G>C
|
ENSP00000501161.2:p.Gly519Ala
|
|
ENST00000710286.1:c.1913G>C
|
ENSP00000518176.1:p.Gly638Ala
|
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ENST00000673903.1:c.1181G>C
|
ENSP00000501257.1:p.Gly394Ala
|
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ENST00000673913.1:c.296G>C
|
ENSP00000501161.1:p.Gly99Ala
|
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ENST00000302118.5:c.1556G>C
MANE Select
|
ENSP00000303208.5:p.Gly519Ala
|
|
ENST00000490692.1:n.2227+891G>C
|
|
|
NM_174936.3:c.1556G>C , LRG_275t1:c.1556G>C
|
NP_777596.2:p.Gly519Ala
|
|
NR_110451.1:n.1163G>C
|
|
|
XM_011541193.1:c.677G>C
|
XP_011539495.1:p.Gly226Ala
|
|
NM_174936.4:c.1556G>C
MANE Select
|
NP_777596.2:p.Gly519Ala
|
|
NR_110451.2:n.1163G>C
|
|
|