ENST00000593677.2:c.858A=
|
|
|
ENST00000688602.1:c.2255A=
|
|
|
ENST00000689936.1:c.2227A=
|
|
|
ENST00000359596.8:c.13922A=
MANE Select
|
ENSP00000352608.2:p.Glu4641=
|
|
ENST00000355481.8:c.13907A=
|
ENSP00000347667.3:p.Glu4636=
|
|
ENST00000359596.7:c.13922A=
|
ENSP00000352608.2:p.Glu4641=
|
|
ENST00000360985.7:c.13904A=
|
ENSP00000354254.4:p.Glu4635=
|
|
ENST00000593677.1:c.382A=
|
|
|
NM_000540.2:c.13922A= , LRG_766t1:c.13922A=
|
NP_000531.2:p.Glu4641=
|
|
NM_001042723.1:c.13907A=
|
NP_001036188.1:p.Glu4636=
|
|
XM_006723317.1:c.13904A=
|
XP_006723380.1:p.Glu4635=
|
|
XM_006723319.1:c.13889A=
|
XP_006723382.1:p.Glu4630=
|
|
XM_011527204.1:c.13919A=
|
XP_011525506.1:p.Glu4640=
|
|
XM_011527205.1:c.13835A=
|
XP_011525507.1:p.Glu4612=
|
|
XM_006723317.2:c.13904A=
|
XP_006723380.1:p.Glu4635=
|
|
XM_006723319.2:c.13889A=
|
XP_006723382.1:p.Glu4630=
|
|
XM_011527205.2:c.13835A=
|
XP_011525507.1:p.Glu4612=
|
|
NM_000540.3:c.13922A=
MANE Select
|
NP_000531.2:p.Glu4641=
|
|
NM_001042723.2:c.13907A=
|
NP_001036188.1:p.Glu4636=
|
|