NM_000110.4:c.2872A>G
MANE Select
|
NP_000101.2:p.Lys958Glu
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ENST00000370192.8:c.2872A>G
MANE Select
|
ENSP00000359211.3:p.Lys958Glu
|
NM_000110.3:c.2872A>G , LRG_722t1:c.2872A>G
|
NP_000101.2:p.Lys958Glu
|
ENST00000370192.7:c.2872A>G
|
ENSP00000359211.3:p.Lys958Glu
|
XM_005270562.3:c.2656A>G
|
XP_005270619.2:p.Lys886Glu
|
XM_017000507.1:c.2761A>G
|
XP_016855996.1:p.Lys921Glu
|
XM_017000508.2:c.2377A>G
|
XP_016855997.1:p.Lys793Glu
|
XM_017000509.2:c.2377A>G
|
XP_016855998.1:p.Lys793Glu
|
XM_017000510.1:c.2377A>G
|
XP_016855999.1:p.Lys793Glu
|