ENST00000491302.2:n.1679G>A
|
|
|
ENST00000697630.1:n.6456G>A
|
|
|
ENST00000697631.1:c.2341G>A
|
ENSP00000513363.1:p.Glu781Lys
|
|
ENST00000697632.1:c.1588G>A
|
ENSP00000513364.1:p.Glu530Lys
|
|
ENST00000697633.1:c.1233G>A
|
|
|
ENST00000348564.11:c.2143G>A
|
ENSP00000306782.7:p.Glu715Lys
|
|
ENST00000442510.8:c.2626G>A
MANE Select
|
ENSP00000411355.3:p.Glu876Lys
|
|
ENST00000348564.10:c.2143G>A
|
ENSP00000306782.7:p.Glu715Lys
|
|
ENST00000442510.6:c.2626G>A
|
ENSP00000411355.3:p.Glu876Lys
|
|
NM_002838.4:c.2626G>A
|
NP_002829.3:p.Glu876Lys
|
|
NM_080921.3:c.2143G>A
|
NP_563578.2:p.Glu715Lys
|
|
XM_006711472.2:c.2482G>A
|
XP_006711535.1:p.Glu828Lys
|
|
XM_006711473.2:c.2428G>A
|
XP_006711536.1:p.Glu810Lys
|
|
XM_006711474.2:c.2284G>A
|
XP_006711537.1:p.Glu762Lys
|
|
XM_006711472.4:c.2482G>A
|
XP_006711535.1:p.Glu828Lys
|
|
XM_006711473.3:c.2428G>A
|
XP_006711536.1:p.Glu810Lys
|
|
XM_006711474.3:c.2284G>A
|
XP_006711537.1:p.Glu762Lys
|
|
NM_002838.5:c.2626G>A
MANE Select
|
NP_002829.3:p.Glu876Lys
|
|
NM_080921.4:c.2143G>A
|
NP_563578.2:p.Glu715Lys
|
|