ENST00000355943.8:c.387T>A
MANE Select
|
ENSP00000348211.3:p.Val129=
|
|
ENST00000355943.7:c.387T>A
|
ENSP00000348211.3:p.Val129=
|
|
ENST00000447245.6:c.387T>A
|
ENSP00000399717.2:p.Val129=
|
|
ENST00000502462.6:n.703T>A
|
|
|
ENST00000504098.1:c.-52T>A
|
ENSP00000425708.1:n.-52T>A
|
|
ENST00000508781.5:n.216T>A
|
|
|
ENST00000513807.5:c.-100T>A
|
ENSP00000421134.1:n.-100T>A
|
|
NM_001303249.1:c.387T>A
|
NP_001290178.1:p.Val129=
|
|
NM_001303250.1:c.114T>A
|
NP_001290179.1:p.Val38=
|
|
NM_138773.2:c.387T>A
|
NP_620128.1:p.Val129=
|
|
XM_011543708.1:c.387T>A
|
XP_011542010.1:p.Val129=
|
|
NM_001303249.2:c.387T>A
|
NP_001290178.1:p.Val129=
|
|
NM_001303250.2:c.114T>A
|
NP_001290179.1:p.Val38=
|
|
NM_138773.3:c.387T>A
|
NP_620128.1:p.Val129=
|
|
NR_138151.1:n.535T>A
|
|
|
NM_138773.4:c.387T>A
MANE Select
|
NP_620128.1:p.Val129=
|
|
NM_001303249.3:c.387T>A
|
NP_001290178.1:p.Val129=
|
|
NM_001303250.3:c.114T>A
|
NP_001290179.1:p.Val38=
|
|
NR_138151.2:n.500T>A
|
|
|