ENST00000264414.9:c.1254T>G
MANE Select
|
ENSP00000264414.4:p.Leu418=
|
|
ENST00000264414.8:c.1254T>G
|
ENSP00000264414.4:p.Leu418=
|
|
ENST00000344951.8:c.1056T>G
|
ENSP00000343601.4:p.Leu352=
|
|
ENST00000409096.5:c.1182T>G
|
ENSP00000387200.1:p.Leu394=
|
|
ENST00000409777.5:c.1182T>G
|
ENSP00000386525.1:p.Leu394=
|
|
ENST00000481135.1:n.550T>G
|
|
|
ENST00000617432.4:c.-23T>G
|
ENSP00000477851.1:n.-23T>G
|
|
NM_001257197.1:c.1056T>G
|
NP_001244126.1:p.Leu352=
|
|
NM_001257198.1:c.1272T>G
|
NP_001244127.1:p.Leu424=
|
|
NM_003590.4:c.1254T>G
|
NP_003581.1:p.Leu418=
|
|
XM_006712800.2:c.1221T>G
|
XP_006712863.2:p.Leu407=
|
|
XM_011511994.1:c.1107T>G
|
XP_011510296.1:p.Leu369=
|
|
XM_011511995.1:c.1212T>G
|
XP_011510297.1:p.Leu404=
|
|
XM_011511996.1:c.1062T>G
|
XP_011510298.1:p.Leu354=
|
|
XM_011511997.1:c.954T>G
|
XP_011510299.1:p.Leu318=
|
|
XM_011511994.3:c.1107T>G
|
XP_011510296.1:p.Leu369=
|
|
XM_011511996.2:c.1062T>G
|
XP_011510298.1:p.Leu354=
|
|
NM_003590.5:c.1254T>G
MANE Select
|
NP_003581.1:p.Leu418=
|
|
NM_001257198.2:c.1272T>G
|
NP_001244127.1:p.Leu424=
|
|
NM_001257197.2:c.1056T>G
|
NP_001244126.1:p.Leu352=
|
|