ENST00000461271.6:c.33T>C
|
ENSP00000464056.2:p.Gly11=
|
|
ENST00000697675.1:n.1478T>C
|
|
|
ENST00000697676.1:n.444T>C
|
|
|
ENST00000697677.1:n.1465T>C
|
|
|
ENST00000697678.1:n.286T>C
|
|
|
ENST00000697679.1:n.1458T>C
|
|
|
ENST00000697680.1:c.*1248T>C
|
ENSP00000513392.1:n.*1248T>C
|
|
ENST00000697681.1:c.*1248T>C
|
ENSP00000513393.1:n.*1248T>C
|
|
ENST00000697683.1:c.*1248T>C
|
ENSP00000513395.1:n.*1248T>C
|
|
ENST00000697684.1:n.444T>C
|
|
|
ENST00000697685.1:c.*1248T>C
|
ENSP00000513396.1:n.*1248T>C
|
|
ENST00000697686.1:c.33T>C
|
ENSP00000513397.1:p.Gly11=
|
|
ENST00000697687.1:n.430T>C
|
|
|
ENST00000697688.1:n.430T>C
|
|
|
ENST00000697689.1:c.*1087T>C
|
ENSP00000513398.1:n.*1087T>C
|
|
ENST00000697690.1:c.384T>C
|
ENSP00000513399.1:p.Gly128=
|
|
ENST00000697691.1:c.*356T>C
|
ENSP00000513400.1:n.*356T>C
|
|
ENST00000697692.1:c.*396T>C
|
ENSP00000513401.1:n.*396T>C
|
|
ENST00000697693.1:n.1159T>C
|
|
|
ENST00000697694.1:c.33T>C
|
ENSP00000513402.1:p.Gly11=
|
|
ENST00000697695.1:n.991T>C
|
|
|
ENST00000337432.9:c.384T>C
MANE Select
|
ENSP00000336701.4:p.Gly128=
|
|
ENST00000337432.8:c.384T>C
|
ENSP00000336701.4:p.Gly128=
|
|
ENST00000413590.5:c.22T>C
|
|
|
ENST00000421782.3:c.384T>C
|
ENSP00000391450.2:p.Gly128=
|
|
ENST00000425173.5:c.180T>C
|
ENSP00000407282.1:p.Gly60=
|
|
ENST00000461271.5:c.33T>C
|
ENSP00000464056.1:p.Gly11=
|
|
ENST00000475762.5:c.*1087T>C
|
ENSP00000432421.1:n.*1087T>C
|
|
ENST00000482007.5:c.384T>C
|
ENSP00000433332.1:p.Gly128=
|
|
ENST00000486827.1:c.*1248T>C
|
ENSP00000436761.1:n.*1248T>C
|
|
ENST00000487525.5:c.384T>C
|
ENSP00000431637.1:p.Gly128=
|
|
ENST00000487921.5:n.296T>C
|
|
|
ENST00000583539.5:c.384T>C
|
ENSP00000463121.1:p.Gly128=
|
|
ENST00000584617.5:c.127-1524T>C
|
|
|
ENST00000622327.4:c.120T>C
|
ENSP00000482326.1:p.Gly40=
|
|
NM_002876.3:c.384T>C
|
NP_002867.1:p.Gly128=
|
|
NM_058216.2:c.384T>C
|
NP_478123.1:p.Gly128=
|
|
NR_103872.1:n.455T>C
|
|
|
NR_103873.1:n.352T>C
|
|
|
XM_006722001.2:c.384T>C
|
XP_006722064.1:p.Gly128=
|
|
XM_006722002.2:c.384T>C
|
XP_006722065.1:p.Gly128=
|
|
XM_006722004.2:c.33T>C
|
XP_006722067.1:p.Gly11=
|
|
XM_006722005.2:c.33T>C
|
XP_006722068.1:p.Gly11=
|
|
XM_011525092.1:c.33T>C
|
XP_011523394.1:p.Gly11=
|
|
XM_011525093.1:c.33T>C
|
XP_011523395.1:p.Gly11=
|
|
XM_011525094.1:c.33T>C
|
XP_011523396.1:p.Gly11=
|
|
XR_934513.1:n.457T>C
|
|
|
XR_934514.1:n.457T>C
|
|
|
XM_006722001.4:c.384T>C
|
XP_006722064.1:p.Gly128=
|
|
XM_006722002.4:c.384T>C
|
XP_006722065.1:p.Gly128=
|
|
XM_006722004.3:c.33T>C
|
XP_006722067.1:p.Gly11=
|
|
XM_006722005.3:c.33T>C
|
XP_006722068.1:p.Gly11=
|
|
XM_011525092.2:c.33T>C
|
XP_011523394.1:p.Gly11=
|
|
XM_011525093.2:c.33T>C
|
XP_011523395.1:p.Gly11=
|
|
XM_011525094.2:c.33T>C
|
XP_011523396.1:p.Gly11=
|
|
XM_017024914.1:c.33T>C
|
XP_016880403.1:p.Gly11=
|
|
XM_017024915.1:c.33T>C
|
XP_016880404.1:p.Gly11=
|
|
XM_017024916.1:c.33T>C
|
XP_016880405.1:p.Gly11=
|
|
XM_017024917.1:c.33T>C
|
XP_016880406.1:p.Gly11=
|
|
XM_017024918.2:c.33T>C
|
XP_016880407.1:p.Gly11=
|
|
XM_017024919.1:c.33T>C
|
XP_016880408.1:p.Gly11=
|
|
XR_934513.3:n.888T>C
|
|
|
XR_934514.3:n.888T>C
|
|
|
NM_058216.3:c.384T>C
MANE Select
|
NP_478123.1:p.Gly128=
|
|
NR_103872.2:n.426T>C
|
|
|
NM_002876.4:c.384T>C
|
NP_002867.1:p.Gly128=
|
|