ENST00000324856.13:c.5300A=
MANE Select
|
ENSP00000320485.7:p.Glu1767=
|
|
ENST00000374152.7:c.4151A=
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ENSP00000363267.2:p.Glu1384=
|
|
ENST00000430799.7:c.4148A=
|
ENSP00000390317.3:p.Glu1383=
|
|
ENST00000466382.2:c.717A=
|
|
|
ENST00000636219.1:c.4154A=
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ENSP00000489842.1:p.Glu1385=
|
|
ENST00000637788.1:n.1100A=
|
|
|
ENST00000324856.11:c.5300A=
|
ENSP00000320485.7:p.Glu1767=
|
|
ENST00000374152.6:c.4151A=
|
ENSP00000363267.2:p.Glu1384=
|
|
ENST00000430799.6:c.1989A=
|
|
|
ENST00000457599.6:c.4649A=
|
ENSP00000387636.2:p.Glu1550=
|
|
ENST00000466382.1:c.717A=
|
|
|
ENST00000532781.1:c.798A=
|
|
|
NM_006015.4:c.5300A= , LRG_875t1:c.5300A=
|
NP_006006.3:p.Glu1767=
|
|
NM_139135.2:c.4649A=
|
NP_624361.1:p.Glu1550=
|
|
NM_006015.5:c.5300A=
|
NP_006006.3:p.Glu1767=
|
|
NM_139135.3:c.4649A=
|
NP_624361.1:p.Glu1550=
|
|
NM_006015.6:c.5300A=
MANE Select
|
NP_006006.3:p.Glu1767=
|
|
NM_139135.4:c.4649A=
|
NP_624361.1:p.Glu1550=
|
|