ENST00000400521.7:c.782C=
MANE Select
|
ENSP00000383365.1:p.Ser261=
|
|
ENST00000334363.14:c.782C=
|
ENSP00000334451.9:p.Ser261=
|
|
ENST00000400518.5:c.692C=
|
ENSP00000383362.1:p.Ser231=
|
|
ENST00000400519.6:c.779C=
|
ENSP00000383363.1:p.Ser260=
|
|
ENST00000400521.6:c.782C=
|
ENSP00000383365.1:p.Ser261=
|
|
ENST00000400525.6:c.713C=
|
ENSP00000383369.3:p.Ser238=
|
|
ENST00000474308.5:c.725C=
|
ENSP00000485665.1:p.Ser242=
|
|
ENST00000475995.3:c.279C=
|
|
|
ENST00000491939.6:c.686C=
|
ENSP00000485543.1:p.Ser229=
|
|
ENST00000494454.5:n.856C=
|
|
|
ENST00000542719.6:c.494C=
|
ENSP00000485128.2:p.Ser165=
|
|
ENST00000634537.1:c.11C=
|
ENSP00000489208.1:p.Ser4=
|
|
ENST00000635155.1:n.368C=
|
|
|
NM_001282512.1:c.782C=
|
NP_001269441.1:p.Ser261=
|
|
NM_006440.4:c.782C=
|
NP_006431.2:p.Ser261=
|
|
NM_001282512.2:c.782C=
|
NP_001269441.1:p.Ser261=
|
|
NM_001352300.1:c.779C=
|
NP_001339229.1:p.Ser260=
|
|
NM_001352301.1:c.692C=
|
NP_001339230.1:p.Ser231=
|
|
NM_001352302.1:c.494C=
|
NP_001339231.1:p.Ser165=
|
|
NM_001352303.1:c.686C=
|
NP_001339232.1:p.Ser229=
|
|
NR_147957.1:n.914C=
|
|
|
NM_006440.5:c.782C=
MANE Select
|
NP_006431.2:p.Ser261=
|
|
NM_001282512.3:c.782C=
|
NP_001269441.1:p.Ser261=
|
|
NM_001352300.2:c.779C=
|
NP_001339229.1:p.Ser260=
|
|
NR_147957.2:n.740C=
|
|
|
NM_001352301.2:c.692C=
|
NP_001339230.1:p.Ser231=
|
|
NM_001352302.2:c.494C=
|
NP_001339231.1:p.Ser165=
|
|
NM_001352303.2:c.686C=
|
NP_001339232.1:p.Ser229=
|
|