ENST00000400521.7:c.860T=
MANE Select
|
ENSP00000383365.1:p.Leu287=
|
|
ENST00000334363.14:c.860T=
|
ENSP00000334451.9:p.Leu287=
|
|
ENST00000400518.5:c.770T=
|
ENSP00000383362.1:p.Leu257=
|
|
ENST00000400519.6:c.857T=
|
ENSP00000383363.1:p.Leu286=
|
|
ENST00000400521.6:c.860T=
|
ENSP00000383365.1:p.Leu287=
|
|
ENST00000400525.6:c.791T=
|
ENSP00000383369.3:p.Leu264=
|
|
ENST00000474308.5:c.803T=
|
ENSP00000485665.1:p.Leu268=
|
|
ENST00000475995.3:c.357T=
|
|
|
ENST00000491939.6:c.764T=
|
ENSP00000485543.1:p.Leu255=
|
|
ENST00000494454.5:n.934T=
|
|
|
ENST00000542719.6:c.572T=
|
ENSP00000485128.2:p.Leu191=
|
|
ENST00000634537.1:c.89T=
|
ENSP00000489208.1:p.Leu30=
|
|
ENST00000635155.1:n.446T=
|
|
|
NM_001282512.1:c.860T=
|
NP_001269441.1:p.Leu287=
|
|
NM_006440.4:c.860T=
|
NP_006431.2:p.Leu287=
|
|
NM_001282512.2:c.860T=
|
NP_001269441.1:p.Leu287=
|
|
NM_001352300.1:c.857T=
|
NP_001339229.1:p.Leu286=
|
|
NM_001352301.1:c.770T=
|
NP_001339230.1:p.Leu257=
|
|
NM_001352302.1:c.572T=
|
NP_001339231.1:p.Leu191=
|
|
NM_001352303.1:c.764T=
|
NP_001339232.1:p.Leu255=
|
|
NR_147957.1:n.992T=
|
|
|
NM_006440.5:c.860T=
MANE Select
|
NP_006431.2:p.Leu287=
|
|
NM_001282512.3:c.860T=
|
NP_001269441.1:p.Leu287=
|
|
NM_001352300.2:c.857T=
|
NP_001339229.1:p.Leu286=
|
|
NR_147957.2:n.818T=
|
|
|
NM_001352301.2:c.770T=
|
NP_001339230.1:p.Leu257=
|
|
NM_001352302.2:c.572T=
|
NP_001339231.1:p.Leu191=
|
|
NM_001352303.2:c.764T=
|
NP_001339232.1:p.Leu255=
|
|