ENST00000264414.9:c.1269A>G
MANE Select
|
ENSP00000264414.4:p.Gln423=
|
|
ENST00000264414.8:c.1269A>G
|
ENSP00000264414.4:p.Gln423=
|
|
ENST00000344951.8:c.1071A>G
|
ENSP00000343601.4:p.Gln357=
|
|
ENST00000409096.5:c.1197A>G
|
ENSP00000387200.1:p.Gln399=
|
|
ENST00000409777.5:c.1197A>G
|
ENSP00000386525.1:p.Gln399=
|
|
ENST00000481135.1:n.565A>G
|
|
|
ENST00000617432.4:c.-8A>G
|
ENSP00000477851.1:n.-8A>G
|
|
NM_001257197.1:c.1071A>G
|
NP_001244126.1:p.Gln357=
|
|
NM_001257198.1:c.1287A>G
|
NP_001244127.1:p.Gln429=
|
|
NM_003590.4:c.1269A>G
|
NP_003581.1:p.Gln423=
|
|
XM_006712800.2:c.1236A>G
|
XP_006712863.2:p.Gln412=
|
|
XM_011511994.1:c.1122A>G
|
XP_011510296.1:p.Gln374=
|
|
XM_011511995.1:c.1227A>G
|
XP_011510297.1:p.Gln409=
|
|
XM_011511996.1:c.1077A>G
|
XP_011510298.1:p.Gln359=
|
|
XM_011511997.1:c.969A>G
|
XP_011510299.1:p.Gln323=
|
|
XM_011511994.3:c.1122A>G
|
XP_011510296.1:p.Gln374=
|
|
XM_011511996.2:c.1077A>G
|
XP_011510298.1:p.Gln359=
|
|
NM_003590.5:c.1269A>G
MANE Select
|
NP_003581.1:p.Gln423=
|
|
NM_001257198.2:c.1287A>G
|
NP_001244127.1:p.Gln429=
|
|
NM_001257197.2:c.1071A>G
|
NP_001244126.1:p.Gln357=
|
|