ENST00000342245.9:c.1131C>G
MANE Select
|
ENSP00000340409.4:p.Leu377=
|
|
ENST00000342245.8:c.1131C>G
|
ENSP00000340409.4:p.Leu377=
|
|
ENST00000526280.1:c.321-362C>G
|
|
|
ENST00000527275.5:c.1128C>G
|
ENSP00000435350.1:p.Leu376=
|
|
ENST00000531303.5:c.478C>G
|
ENSP00000432625.1:p.Pro160Ala
|
|
ENST00000533123.5:c.1092-362C>G
|
ENSP00000435950.1:n.1092-362C>G
|
|
ENST00000534405.5:c.1171C>G
|
ENSP00000434353.1:p.Pro391Ala
|
|
NM_000543.4:c.1131C>G
|
NP_000534.3:p.Leu377=
|
|
NM_001007593.2:c.1128C>G
|
NP_001007594.2:p.Leu376=
|
|
XM_005253075.3:c.1131C>G
|
XP_005253132.1:p.Leu377=
|
|
XM_011520303.1:c.1132-362C>G
|
XP_011518605.1:n.1132-362C>G
|
|
XM_011520304.1:c.1132-362C>G
|
XP_011518606.1:n.1132-362C>G
|
|
XR_930886.1:n.1469C>G
|
|
|
NM_001318087.1:c.1131C>G
|
NP_001305016.1:p.Leu377=
|
|
NM_001318088.1:c.210C>G
|
NP_001305017.1:p.Leu70=
|
|
NM_001365135.1:c.1132-362C>G
|
NP_001352064.1:n.1132-362C>G
|
|
NR_027400.2:n.1277-362C>G
|
|
|
NR_134502.1:n.663C>G
|
|
|
XM_011520304.2:c.1132-362C>G
|
XP_011518606.1:n.1132-362C>G
|
|
XR_001747940.2:n.1296C>G
|
|
|
XR_002957158.1:n.1296C>G
|
|
|
NM_000543.5:c.1131C>G
MANE Select
|
NP_000534.3:p.Leu377=
|
|
NM_001007593.3:c.1128C>G
|
NP_001007594.2:p.Leu376=
|
|
NM_001318087.2:c.1131C>G
|
NP_001305016.1:p.Leu377=
|
|
NM_001318088.2:c.210C>G
|
NP_001305017.1:p.Leu70=
|
|
NM_001365135.2:c.1132-362C>G
|
NP_001352064.1:n.1132-362C>G
|
|
NR_027400.3:n.1217-362C>G
|
|
|
NR_134502.2:n.603C>G
|
|
|