ENST00000465378.6:n.790G>T
|
|
|
ENST00000642923.1:c.637G>T
|
ENSP00000494255.1:p.Glu213Ter
|
|
ENST00000643137.1:c.637G>T
|
ENSP00000495331.1:p.Glu213Ter
|
|
ENST00000644006.1:c.*186G>T
|
ENSP00000493778.1:n.*186G>T
|
|
ENST00000645026.1:n.793G>T
|
|
|
ENST00000645190.1:c.742G>T
MANE Select
|
ENSP00000496496.1:p.Glu248Ter
|
|
ENST00000647301.1:c.*186G>T
|
ENSP00000496641.1:n.*186G>T
|
|
ENST00000290846.8:c.742G>T
|
ENSP00000290846.4:p.Glu248Ter
|
|
ENST00000381019.3:c.742G>T
|
ENSP00000370407.3:p.Glu248Ter
|
|
ENST00000381021.7:c.*335G>T
|
ENSP00000370409.3:n.*335G>T
|
|
ENST00000441818.5:c.*276G>T
|
ENSP00000393014.1:n.*276G>T
|
|
ENST00000453630.5:c.*280G>T
|
ENSP00000398488.1:n.*280G>T
|
|
ENST00000456595.5:c.*276G>T
|
ENSP00000413880.1:n.*276G>T
|
|
ENST00000457572.5:c.*186G>T
|
ENSP00000407700.1:n.*186G>T
|
|
ENST00000463785.1:n.210G>T
|
|
|
ENST00000479648.1:n.562G>T
|
|
|
ENST00000485175.5:n.702G>T
|
|
|
ENST00000486620.5:n.784G>T
|
|
|
NM_001282782.1:c.400G>T
|
NP_001269711.1:p.Glu134Ter
|
|
NM_001282783.1:c.322G>T
|
NP_001269712.1:p.Glu108Ter
|
|
NM_001282784.1:c.322G>T
|
NP_001269713.1:p.Glu108Ter
|
|
NM_001282785.1:c.742G>T
|
NP_001269714.1:p.Glu248Ter
|
|
NM_018006.4:c.742G>T
|
NP_060476.2:p.Glu248Ter
|
|
NR_104240.1:n.1051G>T
|
|
|
NR_104241.1:n.944G>T
|
|
|
XM_005261678.1:c.346G>T
|
XP_005261735.1:p.Glu116Ter
|
|
XM_005261681.1:c.346G>T
|
XP_005261738.1:p.Glu116Ter
|
|
XM_011530271.1:c.637G>T
|
XP_011528573.1:p.Glu213Ter
|
|
XM_011530272.1:c.742G>T
|
XP_011528574.1:p.Glu248Ter
|
|
XM_011530273.1:c.742G>T
|
XP_011528575.1:p.Glu248Ter
|
|
XM_011530274.1:c.400G>T
|
XP_011528576.1:p.Glu134Ter
|
|
XM_011530275.1:c.346G>T
|
XP_011528577.1:p.Glu116Ter
|
|
XM_011530271.2:c.637G>T
|
XP_011528573.1:p.Glu213Ter
|
|
XM_011530272.2:c.742G>T
|
XP_011528574.1:p.Glu248Ter
|
|
XM_011530273.2:c.742G>T
|
XP_011528575.1:p.Glu248Ter
|
|
XM_011530274.2:c.400G>T
|
XP_011528576.1:p.Glu134Ter
|
|
XM_024452260.1:c.637G>T
|
XP_024308028.1:p.Glu213Ter
|
|
XR_001755261.2:n.788G>T
|
|
|
XR_001755262.2:n.788G>T
|
|
|
NM_018006.5:c.742G>T
MANE Select
|
NP_060476.2:p.Glu248Ter
|
|
NM_001282782.2:c.400G>T
|
NP_001269711.1:p.Glu134Ter
|
|
NM_001282783.2:c.322G>T
|
NP_001269712.1:p.Glu108Ter
|
|
NM_001282784.2:c.322G>T
|
NP_001269713.1:p.Glu108Ter
|
|
NM_001282785.2:c.742G>T
|
NP_001269714.1:p.Glu248Ter
|
|
NR_104240.2:n.738G>T
|
|
|
NR_104241.2:n.631G>T
|
|
|