ENST00000355112.8:c.3123T>G
MANE Select
|
ENSP00000347232.3:p.Leu1041=
|
|
ENST00000560559.2:n.1696T>G
|
|
|
ENST00000648453.1:c.3123T>G
|
ENSP00000497646.1:p.Leu1041=
|
|
ENST00000680772.1:c.3123T>G
|
ENSP00000506117.1:p.Leu1041=
|
|
ENST00000681142.1:c.3123T>G
|
ENSP00000506682.1:p.Leu1041=
|
|
ENST00000355112.7:c.3123T>G
|
ENSP00000347232.3:p.Leu1041=
|
|
ENST00000558825.5:n.470T>G
|
|
|
ENST00000559724.5:c.*2047T>G
|
ENSP00000453359.1:n.*2047T>G
|
|
ENST00000560136.5:n.1149T>G
|
|
|
ENST00000560509.5:c.3123T>G
|
ENSP00000454158.1:p.Leu1041=
|
|
ENST00000560559.1:n.660T>G
|
|
|
NM_000057.3:c.3123T>G
|
NP_000048.1:p.Leu1041=
|
|
NM_001287246.1:c.3123T>G
|
NP_001274175.1:p.Leu1041=
|
|
NM_001287247.1:c.3123T>G
|
NP_001274176.1:p.Leu1041=
|
|
NM_001287248.1:c.1998T>G
|
NP_001274177.1:p.Leu666=
|
|
XM_006720632.2:c.1161T>G
|
XP_006720695.1:p.Leu387=
|
|
XM_011521881.1:c.1809T>G
|
XP_011520183.1:p.Leu603=
|
|
XM_011521881.2:c.1809T>G
|
XP_011520183.1:p.Leu603=
|
|
NM_000057.4:c.3123T>G
MANE Select
|
NP_000048.1:p.Leu1041=
|
|
NM_001287246.2:c.3123T>G
|
NP_001274175.1:p.Leu1041=
|
|
NM_001287247.2:c.3123T>G
|
NP_001274176.1:p.Leu1041=
|
|
NM_001287248.2:c.1998T>G
|
NP_001274177.1:p.Leu666=
|
|