ENST00000373207.2:c.2967G=
MANE Select
|
ENSP00000362303.1:p.Gln989=
|
|
ENST00000373207.1:c.2967G=
|
ENSP00000362303.1:p.Gln989=
|
|
ENST00000373208.5:c.2976G=
|
ENSP00000362304.1:p.Gln992=
|
|
NM_080722.3:c.2967G=
|
NP_542453.2:p.Gln989=
|
|
NM_139155.2:c.2976G=
|
NP_631894.2:p.Gln992=
|
|
XM_011539300.1:c.2466G=
|
XP_011537602.1:p.Gln822=
|
|
XM_011539301.1:c.2040G=
|
XP_011537603.1:p.Gln680=
|
|
XM_011539302.1:c.2040G=
|
XP_011537604.1:p.Gln680=
|
|
XM_011539308.1:c.*46G=
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XP_011537610.1:n.*46G=
|
|
XM_011539309.1:c.1536G=
|
XP_011537611.1:p.Gln512=
|
|
NM_080722.4:c.2967G=
MANE Select
|
NP_542453.2:p.Gln989=
|
|
NM_139155.3:c.2976G=
|
NP_631894.2:p.Gln992=
|
|
XM_011539300.2:c.2466G=
|
XP_011537602.1:p.Gln822=
|
|
XM_011539301.2:c.2040G=
|
XP_011537603.1:p.Gln680=
|
|
XM_011539302.2:c.2040G=
|
XP_011537604.1:p.Gln680=
|
|
XM_011539308.2:c.*46G=
|
XP_011537610.1:n.*46G=
|
|