ENST00000338946.11:c.2081A>T
|
ENSP00000340051.7:p.Glu694Val
|
|
ENST00000396282.7:c.2384A>T
|
ENSP00000379578.3:p.Glu795Val
|
|
ENST00000686349.1:c.*839A>T
|
ENSP00000510424.1:n.*839A>T
|
|
ENST00000687764.1:c.*1826A>T
|
ENSP00000509967.1:n.*1826A>T
|
|
ENST00000691629.1:n.1748A>T
|
|
|
ENST00000338154.11:c.2384A>T
MANE Select
|
ENSP00000338868.6:p.Glu795Val
|
|
ENST00000322659.12:c.2333A>T
|
ENSP00000319473.8:p.Glu778Val
|
|
ENST00000338154.10:c.2384A>T
|
ENSP00000338868.6:p.Glu795Val
|
|
ENST00000338946.10:c.2081A>T
|
ENSP00000340051.6:p.Glu694Val
|
|
ENST00000357988.9:c.2492A>T
|
ENSP00000350676.5:p.Glu831Val
|
|
ENST00000396282.6:c.2095A>T
|
|
|
ENST00000443302.5:c.1674A>T
|
|
|
ENST00000615775.4:c.811A>T
|
ENSP00000482159.1:p.Arg271Ter
|
|
NM_001184896.1:c.2492A>T
|
NP_001171825.1:p.Glu831Val
|
|
NM_001184897.1:c.2081A>T
|
NP_001171826.1:p.Glu694Val
|
|
NM_001184898.1:c.2333A>T
|
NP_001171827.1:p.Glu778Val
|
|
NM_015107.2:c.2384A>T
|
NP_055922.1:p.Glu795Val
|
|
XM_005261996.1:c.2492A>T
|
XP_005262053.1:p.Glu831Val
|
|
XM_005261997.2:c.2384A>T
|
XP_005262054.1:p.Glu795Val
|
|
XM_005261999.1:c.2384A>T
|
XP_005262056.1:p.Glu795Val
|
|
XM_005262000.1:c.2189A>T
|
XP_005262057.1:p.Glu730Val
|
|
XM_006724585.1:c.2492A>T
|
XP_006724648.1:p.Glu831Val
|
|
XM_011530778.1:c.2492A>T
|
XP_011529080.1:p.Glu831Val
|
|
XM_005261997.4:c.2384A>T
|
XP_005262054.1:p.Glu795Val
|
|
XM_017029361.2:c.2384A>T
|
XP_016884850.1:p.Glu795Val
|
|
XM_017029362.2:c.2384A>T
|
XP_016884851.1:p.Glu795Val
|
|
NM_001184898.2:c.2333A>T
|
NP_001171827.1:p.Glu778Val
|
|
NM_015107.3:c.2384A>T
MANE Select
|
NP_055922.1:p.Glu795Val
|
|
NM_001184897.2:c.2081A>T
|
NP_001171826.1:p.Glu694Val
|
|