ENST00000264414.9:c.1299A>G
MANE Select
|
ENSP00000264414.4:p.Lys433=
|
|
ENST00000264414.8:c.1299A>G
|
ENSP00000264414.4:p.Lys433=
|
|
ENST00000344951.8:c.1101A>G
|
ENSP00000343601.4:p.Lys367=
|
|
ENST00000409096.5:c.1227A>G
|
ENSP00000387200.1:p.Lys409=
|
|
ENST00000409777.5:c.1227A>G
|
ENSP00000386525.1:p.Lys409=
|
|
ENST00000481135.1:n.595A>G
|
|
|
ENST00000617432.4:c.23A>G
|
ENSP00000477851.1:p.Asn8Ser
|
|
NM_001257197.1:c.1101A>G
|
NP_001244126.1:p.Lys367=
|
|
NM_001257198.1:c.1317A>G
|
NP_001244127.1:p.Lys439=
|
|
NM_003590.4:c.1299A>G
|
NP_003581.1:p.Lys433=
|
|
XM_006712800.2:c.1266A>G
|
XP_006712863.2:p.Lys422=
|
|
XM_011511994.1:c.1152A>G
|
XP_011510296.1:p.Lys384=
|
|
XM_011511995.1:c.1257A>G
|
XP_011510297.1:p.Lys419=
|
|
XM_011511996.1:c.1107A>G
|
XP_011510298.1:p.Lys369=
|
|
XM_011511997.1:c.999A>G
|
XP_011510299.1:p.Lys333=
|
|
XM_011511994.3:c.1152A>G
|
XP_011510296.1:p.Lys384=
|
|
XM_011511996.2:c.1107A>G
|
XP_011510298.1:p.Lys369=
|
|
NM_003590.5:c.1299A>G
MANE Select
|
NP_003581.1:p.Lys433=
|
|
NM_001257198.2:c.1317A>G
|
NP_001244127.1:p.Lys439=
|
|
NM_001257197.2:c.1101A>G
|
NP_001244126.1:p.Lys367=
|
|