ENST00000526189.3:c.612T=
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ENSP00000488104.2:p.Ala204=
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|
ENST00000533357.5:c.693T=
MANE Select
|
ENSP00000432943.1:p.Ala231=
|
|
ENST00000672287.2:c.105T=
|
ENSP00000499818.2:p.Ala35=
|
|
ENST00000672602.2:c.693T=
|
ENSP00000500814.2:p.Ala231=
|
|
ENST00000674861.1:n.756T=
|
|
|
ENST00000463290.5:c.693T=
|
ENSP00000431538.1:p.Ala231=
|
|
ENST00000476410.1:n.283T=
|
|
|
ENST00000488271.1:n.131T=
|
|
|
ENST00000491222.5:c.105T=
|
ENSP00000431441.1:p.Ala35=
|
|
ENST00000526189.2:c.356T=
|
|
|
ENST00000533357.4:c.693T=
|
ENSP00000432943.1:p.Ala231=
|
|
NM_000530.6:c.693T= , LRG_256t1:c.693T=
|
NP_000521.2:p.Ala231=
|
|
NM_000530.7:c.693T=
|
NP_000521.2:p.Ala231=
|
|
NM_001315491.1:c.693T=
|
NP_001302420.1:p.Ala231=
|
|
XM_017001321.2:c.675+178T=
|
XP_016856810.1:n.675+178T=
|
|
NM_000530.8:c.693T=
MANE Select
|
NP_000521.2:p.Ala231=
|
|
NM_001315491.2:c.693T=
|
NP_001302420.1:p.Ala231=
|
|