ENST00000681993.1:n.603A>G
|
|
|
ENST00000682295.1:c.303+134A>G
|
ENSP00000507499.1:n.303+134A>G
|
|
ENST00000682303.1:c.*2837A>G
|
ENSP00000508325.1:n.*2837A>G
|
|
ENST00000682308.1:c.3051A>G
|
ENSP00000507056.1:p.Glu1017=
|
|
ENST00000682480.1:c.3069A>G
|
ENSP00000508344.1:p.Glu1023=
|
|
ENST00000682546.1:c.3048A>G
|
ENSP00000508188.1:p.Glu1016=
|
|
ENST00000682585.1:c.3051A>G
|
ENSP00000506885.1:p.Glu1017=
|
|
ENST00000682595.1:n.3635A>G
|
|
|
ENST00000682607.1:c.1469A>G
|
|
|
ENST00000682779.1:c.3042A>G
|
ENSP00000507947.1:p.Glu1014=
|
|
ENST00000682845.1:n.2153A>G
|
|
|
ENST00000682885.1:c.3006A>G
|
ENSP00000508036.1:p.Glu1002=
|
|
ENST00000682933.1:n.3125A>G
|
|
|
ENST00000683072.1:n.3635A>G
|
|
|
ENST00000683080.1:n.670A>G
|
|
|
ENST00000683125.1:c.3159A>G
|
ENSP00000507939.1:p.Glu1053=
|
|
ENST00000683213.1:c.3054A>G
|
ENSP00000507751.1:p.Glu1018=
|
|
ENST00000683220.1:c.3081A>G
|
ENSP00000507151.1:p.Glu1027=
|
|
ENST00000683329.1:n.3854A>G
|
|
|
ENST00000683346.1:c.*2926A>G
|
ENSP00000507458.1:n.*2926A>G
|
|
ENST00000683409.1:n.1658A>G
|
|
|
ENST00000683459.1:n.3638A>G
|
|
|
ENST00000683590.1:c.2897-5564A>G
|
ENSP00000506820.1:n.2897-5564A>G
|
|
ENST00000683623.1:c.2958A>G
|
ENSP00000507702.1:p.Glu986=
|
|
ENST00000683645.1:n.3602A>G
|
|
|
ENST00000683796.1:c.*2923A>G
|
ENSP00000508221.1:n.*2923A>G
|
|
ENST00000683802.1:n.5976A>G
|
|
|
ENST00000683833.1:c.3042A>G
|
ENSP00000506852.1:p.Glu1014=
|
|
ENST00000683994.1:c.3051A>G
|
ENSP00000507181.1:p.Glu1017=
|
|
ENST00000684290.1:c.*587A>G
|
ENSP00000507243.1:n.*587A>G
|
|
ENST00000684306.1:c.*2964A>G
|
ENSP00000508384.1:n.*2964A>G
|
|
ENST00000684341.1:n.3071A>G
|
|
|
ENST00000684383.1:c.*2689A>G
|
ENSP00000506863.1:n.*2689A>G
|
|
ENST00000684619.1:c.*2923A>G
|
ENSP00000508088.1:n.*2923A>G
|
|
ENST00000684705.1:n.172A>G
|
|
|
ENST00000684743.1:n.4082A>G
|
|
|
ENST00000260665.12:c.3051A>G
MANE Select
|
ENSP00000260665.7:p.Glu1017=
|
|
ENST00000260665.11:c.3051A>G
|
ENSP00000260665.7:p.Glu1017=
|
|
NM_133259.3:c.3051A>G
|
NP_573566.2:p.Glu1017=
|
|
XM_006711915.2:c.2973A>G
|
XP_006711978.1:p.Glu991=
|
|
XM_006711916.2:c.3051A>G
|
XP_006711979.1:p.Glu1017=
|
|
XM_011532473.1:c.3051A>G
|
XP_011530775.1:p.Glu1017=
|
|
XM_011532474.1:c.3051A>G
|
XP_011530776.1:p.Glu1017=
|
|
XM_006711916.3:c.3051A>G
|
XP_006711979.1:p.Glu1017=
|
|
XM_017003117.1:c.2973A>G
|
XP_016858606.1:p.Glu991=
|
|
XR_002958896.1:n.3093A>G
|
|
|
NM_133259.4:c.3051A>G
MANE Select
|
NP_573566.2:p.Glu1017=
|
|