ENST00000400521.7:c.786C>T
MANE Select
|
ENSP00000383365.1:p.Ser262=
|
|
ENST00000334363.14:c.786C>T
|
ENSP00000334451.9:p.Ser262=
|
|
ENST00000400518.5:c.696C>T
|
ENSP00000383362.1:p.Ser232=
|
|
ENST00000400519.6:c.783C>T
|
ENSP00000383363.1:p.Ser261=
|
|
ENST00000400521.6:c.786C>T
|
ENSP00000383365.1:p.Ser262=
|
|
ENST00000400525.6:c.717C>T
|
ENSP00000383369.3:p.Ser239=
|
|
ENST00000474308.5:c.729C>T
|
ENSP00000485665.1:p.Ser243=
|
|
ENST00000475995.3:c.283C>T
|
|
|
ENST00000491939.6:c.690C>T
|
ENSP00000485543.1:p.Ser230=
|
|
ENST00000494454.5:n.860C>T
|
|
|
ENST00000542719.6:c.498C>T
|
ENSP00000485128.2:p.Ser166=
|
|
ENST00000634537.1:c.15C>T
|
ENSP00000489208.1:p.Ser5=
|
|
ENST00000635155.1:n.372C>T
|
|
|
NM_001282512.1:c.786C>T
|
NP_001269441.1:p.Ser262=
|
|
NM_006440.4:c.786C>T
|
NP_006431.2:p.Ser262=
|
|
NM_001282512.2:c.786C>T
|
NP_001269441.1:p.Ser262=
|
|
NM_001352300.1:c.783C>T
|
NP_001339229.1:p.Ser261=
|
|
NM_001352301.1:c.696C>T
|
NP_001339230.1:p.Ser232=
|
|
NM_001352302.1:c.498C>T
|
NP_001339231.1:p.Ser166=
|
|
NM_001352303.1:c.690C>T
|
NP_001339232.1:p.Ser230=
|
|
NR_147957.1:n.918C>T
|
|
|
NM_006440.5:c.786C>T
MANE Select
|
NP_006431.2:p.Ser262=
|
|
NM_001282512.3:c.786C>T
|
NP_001269441.1:p.Ser262=
|
|
NM_001352300.2:c.783C>T
|
NP_001339229.1:p.Ser261=
|
|
NR_147957.2:n.744C>T
|
|
|
NM_001352301.2:c.696C>T
|
NP_001339230.1:p.Ser232=
|
|
NM_001352302.2:c.498C>T
|
NP_001339231.1:p.Ser166=
|
|
NM_001352303.2:c.690C>T
|
NP_001339232.1:p.Ser230=
|
|