|
NM_001754.5:c.1416G>A
MANE Select
|
NP_001745.2:p.Leu472=
|
|
ENST00000675419.1:c.1416G>A
MANE Select
|
ENSP00000501943.1:p.Leu472=
|
|
NM_001001890.2:c.1335G>A
|
NP_001001890.1:p.Leu445=
|
|
NM_001001890.3:c.1335G>A
|
NP_001001890.1:p.Leu445=
|
|
NM_001754.4:c.1416G>A , LRG_482t1:c.1416G>A
|
NP_001745.2:p.Leu472=
|
|
ENST00000300305.7:c.1416G>A
|
ENSP00000300305.3:p.Leu472=
|
|
ENST00000344691.8:c.1335G>A
|
ENSP00000340690.4:p.Leu445=
|
|
ENST00000399240.5:c.1143G>A
|
ENSP00000382184.1:p.Leu381=
|
|
ENST00000437180.5:c.1416G>A
|
ENSP00000409227.1:p.Leu472=
|
|
ENST00000482318.5:c.*1006G>A
|
ENSP00000477067.1:n.*1006G>A
|
|
XM_005261068.3:c.1380G>A
|
XP_005261125.1:p.Leu460=
|
|
XM_005261069.3:c.1224G>A
|
XP_005261126.1:p.Leu408=
|
|
XM_005261069.4:c.1224G>A
|
XP_005261126.1:p.Leu408=
|
|
XM_011529766.1:c.1416G>A
|
XP_011528068.1:p.Leu472=
|
|
XM_011529766.2:c.1416G>A
|
XP_011528068.1:p.Leu472=
|
|
XM_011529767.1:c.1377G>A
|
XP_011528069.1:p.Leu459=
|
|
XM_011529767.2:c.1377G>A
|
XP_011528069.1:p.Leu459=
|
|
XM_011529768.1:c.1185G>A
|
XP_011528070.1:p.Leu395=
|
|
XM_011529768.2:c.1185G>A
|
XP_011528070.1:p.Leu395=
|
|
XM_017028487.1:c.1263G>A
|
XP_016883976.1:p.Leu421=
|
