ENST00000400521.7:c.1143G>C
MANE Select
|
ENSP00000383365.1:p.Arg381=
|
|
ENST00000400518.5:c.1053G>C
|
ENSP00000383362.1:p.Arg351=
|
|
ENST00000400519.6:c.1140G>C
|
ENSP00000383363.1:p.Arg380=
|
|
ENST00000400521.6:c.1143G>C
|
ENSP00000383365.1:p.Arg381=
|
|
ENST00000400525.6:c.1074G>C
|
ENSP00000383369.3:p.Arg358=
|
|
ENST00000462330.5:c.66G>C
|
ENSP00000485603.2:p.Arg22=
|
|
ENST00000462843.2:c.93G>C
|
ENSP00000485466.2:p.Arg31=
|
|
ENST00000474308.5:c.1086G>C
|
ENSP00000485665.1:p.Arg362=
|
|
ENST00000485358.5:c.111G>C
|
ENSP00000485499.2:p.Arg37=
|
|
ENST00000487165.5:n.1237G>C
|
|
|
ENST00000494454.5:n.1217G>C
|
|
|
ENST00000495655.2:n.687G>C
|
|
|
ENST00000542719.6:c.855G>C
|
ENSP00000485128.2:p.Arg285=
|
|
ENST00000634471.1:n.244-390G>C
|
|
|
ENST00000634537.1:c.372G>C
|
ENSP00000489208.1:p.Arg124=
|
|
NM_006440.4:c.1143G>C
|
NP_006431.2:p.Arg381=
|
|
NM_001352300.1:c.1140G>C
|
NP_001339229.1:p.Arg380=
|
|
NM_001352301.1:c.1053G>C
|
NP_001339230.1:p.Arg351=
|
|
NM_001352302.1:c.855G>C
|
NP_001339231.1:p.Arg285=
|
|
NR_147957.1:n.1275G>C
|
|
|
NM_006440.5:c.1143G>C
MANE Select
|
NP_006431.2:p.Arg381=
|
|
NM_001352300.2:c.1140G>C
|
NP_001339229.1:p.Arg380=
|
|
NR_147957.2:n.1101G>C
|
|
|
NM_001352301.2:c.1053G>C
|
NP_001339230.1:p.Arg351=
|
|
NM_001352302.2:c.855G>C
|
NP_001339231.1:p.Arg285=
|
|