ENST00000376091.8:c.1357G>C
MANE Select
|
ENSP00000365259.3:p.Glu453Gln
|
|
ENST00000642383.1:c.607G>C
|
ENSP00000496353.1:p.Glu203Gln
|
|
ENST00000642885.1:c.1147G>C
|
ENSP00000496632.1:p.Glu383Gln
|
|
ENST00000643129.1:c.1644G>C
|
|
|
ENST00000646398.1:c.*532G>C
|
ENSP00000495122.1:n.*532G>C
|
|
ENST00000307367.2:c.1147G>C
|
ENSP00000304257.2:p.Glu383Gln
|
|
ENST00000376088.7:c.1357G>C
|
ENSP00000365256.3:p.Glu453Gln
|
|
ENST00000376091.7:c.1357G>C
|
ENSP00000365259.3:p.Glu453Gln
|
|
ENST00000376108.7:c.1147G>C
|
ENSP00000365276.3:p.Glu383Gln
|
|
NM_000084.4:c.1147G>C
|
NP_000075.1:p.Glu383Gln
|
|
NM_001127898.3:c.1357G>C
|
NP_001121370.1:p.Glu453Gln
|
|
NM_001127899.3:c.1357G>C
|
NP_001121371.1:p.Glu453Gln
|
|
NM_001282163.1:c.1207G>C
|
NP_001269092.1:p.Glu403Gln
|
|
XM_011543888.1:c.1357G>C
|
XP_011542190.1:p.Glu453Gln
|
|
XM_011543889.1:c.1147G>C
|
XP_011542191.1:p.Glu383Gln
|
|
XM_017029257.1:c.1369G>C
|
XP_016884746.1:p.Glu457Gln
|
|
XM_017029258.1:c.1369G>C
|
XP_016884747.1:p.Glu457Gln
|
|
NM_001127898.4:c.1357G>C
MANE Select
|
NP_001121370.1:p.Glu453Gln
|
|
NM_000084.5:c.1147G>C
|
NP_000075.1:p.Glu383Gln
|
|
NM_001127899.4:c.1357G>C
|
NP_001121371.1:p.Glu453Gln
|
|
NM_001282163.2:c.1207G>C
|
NP_001269092.1:p.Glu403Gln
|
|