ENST00000400521.7:c.858G>A
MANE Select
|
ENSP00000383365.1:p.Arg286=
|
|
ENST00000334363.14:c.858G>A
|
ENSP00000334451.9:p.Arg286=
|
|
ENST00000400518.5:c.768G>A
|
ENSP00000383362.1:p.Arg256=
|
|
ENST00000400519.6:c.855G>A
|
ENSP00000383363.1:p.Arg285=
|
|
ENST00000400521.6:c.858G>A
|
ENSP00000383365.1:p.Arg286=
|
|
ENST00000400525.6:c.789G>A
|
ENSP00000383369.3:p.Arg263=
|
|
ENST00000474308.5:c.801G>A
|
ENSP00000485665.1:p.Arg267=
|
|
ENST00000475995.3:c.355G>A
|
|
|
ENST00000491939.6:c.762G>A
|
ENSP00000485543.1:p.Arg254=
|
|
ENST00000494454.5:n.932G>A
|
|
|
ENST00000542719.6:c.570G>A
|
ENSP00000485128.2:p.Arg190=
|
|
ENST00000634537.1:c.87G>A
|
ENSP00000489208.1:p.Arg29=
|
|
ENST00000635155.1:n.444G>A
|
|
|
NM_001282512.1:c.858G>A
|
NP_001269441.1:p.Arg286=
|
|
NM_006440.4:c.858G>A
|
NP_006431.2:p.Arg286=
|
|
NM_001282512.2:c.858G>A
|
NP_001269441.1:p.Arg286=
|
|
NM_001352300.1:c.855G>A
|
NP_001339229.1:p.Arg285=
|
|
NM_001352301.1:c.768G>A
|
NP_001339230.1:p.Arg256=
|
|
NM_001352302.1:c.570G>A
|
NP_001339231.1:p.Arg190=
|
|
NM_001352303.1:c.762G>A
|
NP_001339232.1:p.Arg254=
|
|
NR_147957.1:n.990G>A
|
|
|
NM_006440.5:c.858G>A
MANE Select
|
NP_006431.2:p.Arg286=
|
|
NM_001282512.3:c.858G>A
|
NP_001269441.1:p.Arg286=
|
|
NM_001352300.2:c.855G>A
|
NP_001339229.1:p.Arg285=
|
|
NR_147957.2:n.816G>A
|
|
|
NM_001352301.2:c.768G>A
|
NP_001339230.1:p.Arg256=
|
|
NM_001352302.2:c.570G>A
|
NP_001339231.1:p.Arg190=
|
|
NM_001352303.2:c.762G>A
|
NP_001339232.1:p.Arg254=
|
|