|
ENST00000704289.1:c.*785C>G
|
ENSP00000515816.1:n.*785C>G
|
|
|
ENST00000315285.9:c.1125C>G
MANE Select
|
ENSP00000320885.3:p.Ala375=
|
|
|
ENST00000621856.2:c.1122C>G
|
ENSP00000482496.2:p.Ala374=
|
|
|
ENST00000642281.1:c.983-9589C>G
|
|
|
|
ENST00000642455.1:c.1026C>G
|
ENSP00000493827.1:p.Ala342=
|
|
|
ENST00000642751.1:c.899C>G
|
|
|
|
ENST00000642999.1:c.867C>G
|
ENSP00000496589.1:p.Ala289=
|
|
|
ENST00000643327.1:c.284C>G
|
|
|
|
ENST00000643334.1:c.705C>G
|
|
|
|
ENST00000644408.1:c.1001C>G
|
|
|
|
ENST00000644954.1:c.771C>G
|
ENSP00000494312.1:p.Ala257=
|
|
|
ENST00000645159.1:n.477C>G
|
|
|
|
ENST00000645550.1:n.338C>G
|
|
|
|
ENST00000645671.1:c.575C>G
|
|
|
|
ENST00000645730.1:c.472C>G
|
|
|
|
ENST00000646082.1:c.771C>G
|
|
|
|
ENST00000646571.1:c.1029C>G
|
ENSP00000495015.1:p.Ala343=
|
|
|
ENST00000647007.1:n.817C>G
|
|
|
|
ENST00000647133.1:c.674-1434C>G
|
|
|
|
ENST00000315285.7:c.1125C>G
|
ENSP00000320885.3:p.Ala375=
|
|
|
ENST00000345662.5:c.1029C>G
|
ENSP00000340817.1:p.Ala343=
|
|
|
ENST00000615843.4:c.1125C>G
|
ENSP00000480893.1:p.Ala375=
|
|
|
ENST00000621856.1:c.867C>G
|
ENSP00000482496.1:p.Ala289=
|
|
|
NM_014946.3:c.1125C>G , LRG_714t1:c.1125C>G
|
NP_055761.2:p.Ala375=
|
|
|
NM_199436.1:c.1029C>G
|
NP_955468.1:p.Ala343=
|
|
|
XM_005264516.3:c.1122C>G
|
XP_005264573.1:p.Ala374=
|
|
|
XM_011533067.1:c.1125C>G
|
XP_011531369.1:p.Ala375=
|
|
|
NM_001363823.1:c.1122C>G
|
NP_001350752.1:p.Ala374=
|
|
|
NM_001363875.1:c.1026C>G
|
NP_001350804.1:p.Ala342=
|
|
|
XM_005264516.5:c.1122C>G
|
XP_005264573.1:p.Ala374=
|
|
|
XM_011533067.2:c.1125C>G
|
XP_011531369.1:p.Ala375=
|
|
|
XM_017004778.2:c.1029C>G
|
XP_016860267.1:p.Ala343=
|
|
|
NM_001363823.2:c.1122C>G
|
NP_001350752.1:p.Ala374=
|
|
|
NM_001363875.2:c.1026C>G
|
NP_001350804.1:p.Ala342=
|
|
|
NM_001377959.1:c.1029C>G
|
NP_001364888.1:p.Ala343=
|
|
|
NM_014946.4:c.1125C>G
MANE Select
|
NP_055761.2:p.Ala375=
|
|
|
NM_199436.2:c.1029C>G
|
NP_955468.1:p.Ala343=
|
|
