ENST00000681993.1:n.669A>G
|
|
|
ENST00000682295.1:c.303+200A>G
|
ENSP00000507499.1:n.303+200A>G
|
|
ENST00000682303.1:c.*2903A>G
|
ENSP00000508325.1:n.*2903A>G
|
|
ENST00000682308.1:c.3117A>G
|
ENSP00000507056.1:p.Ile1039Met
|
|
ENST00000682480.1:c.3135A>G
|
ENSP00000508344.1:p.Ile1045Met
|
|
ENST00000682546.1:c.3114A>G
|
ENSP00000508188.1:p.Ile1038Met
|
|
ENST00000682585.1:c.3117A>G
|
ENSP00000506885.1:p.Ile1039Met
|
|
ENST00000682595.1:n.3701A>G
|
|
|
ENST00000682607.1:c.1535A>G
|
|
|
ENST00000682779.1:c.3108A>G
|
ENSP00000507947.1:p.Ile1036Met
|
|
ENST00000682845.1:n.2219A>G
|
|
|
ENST00000682885.1:c.3072A>G
|
ENSP00000508036.1:p.Ile1024Met
|
|
ENST00000682933.1:n.3191A>G
|
|
|
ENST00000683072.1:n.3701A>G
|
|
|
ENST00000683080.1:n.736A>G
|
|
|
ENST00000683125.1:c.3225A>G
|
ENSP00000507939.1:p.Ile1075Met
|
|
ENST00000683213.1:c.3120A>G
|
ENSP00000507751.1:p.Ile1040Met
|
|
ENST00000683220.1:c.3147A>G
|
ENSP00000507151.1:p.Ile1049Met
|
|
ENST00000683329.1:n.3920A>G
|
|
|
ENST00000683346.1:c.*2992A>G
|
ENSP00000507458.1:n.*2992A>G
|
|
ENST00000683409.1:n.1724A>G
|
|
|
ENST00000683459.1:n.3704A>G
|
|
|
ENST00000683590.1:c.2897-5498A>G
|
ENSP00000506820.1:n.2897-5498A>G
|
|
ENST00000683623.1:c.3024A>G
|
ENSP00000507702.1:p.Ile1008Met
|
|
ENST00000683645.1:n.3668A>G
|
|
|
ENST00000683796.1:c.*2989A>G
|
ENSP00000508221.1:n.*2989A>G
|
|
ENST00000683802.1:n.6042A>G
|
|
|
ENST00000683833.1:c.3108A>G
|
ENSP00000506852.1:p.Ile1036Met
|
|
ENST00000683994.1:c.3117A>G
|
ENSP00000507181.1:p.Ile1039Met
|
|
ENST00000684290.1:c.*653A>G
|
ENSP00000507243.1:n.*653A>G
|
|
ENST00000684306.1:c.*3030A>G
|
ENSP00000508384.1:n.*3030A>G
|
|
ENST00000684341.1:n.3137A>G
|
|
|
ENST00000684383.1:c.*2755A>G
|
ENSP00000506863.1:n.*2755A>G
|
|
ENST00000684619.1:c.*2989A>G
|
ENSP00000508088.1:n.*2989A>G
|
|
ENST00000684705.1:n.238A>G
|
|
|
ENST00000684743.1:n.4148A>G
|
|
|
ENST00000260665.12:c.3117A>G
MANE Select
|
ENSP00000260665.7:p.Ile1039Met
|
|
ENST00000260665.11:c.3117A>G
|
ENSP00000260665.7:p.Ile1039Met
|
|
NM_133259.3:c.3117A>G
|
NP_573566.2:p.Ile1039Met
|
|
XM_006711915.2:c.3039A>G
|
XP_006711978.1:p.Ile1013Met
|
|
XM_006711916.2:c.3117A>G
|
XP_006711979.1:p.Ile1039Met
|
|
XM_011532473.1:c.3117A>G
|
XP_011530775.1:p.Ile1039Met
|
|
XM_011532474.1:c.3117A>G
|
XP_011530776.1:p.Ile1039Met
|
|
XM_006711916.3:c.3117A>G
|
XP_006711979.1:p.Ile1039Met
|
|
XM_017003117.1:c.3039A>G
|
XP_016858606.1:p.Ile1013Met
|
|
XR_002958896.1:n.3159A>G
|
|
|
NM_133259.4:c.3117A>G
MANE Select
|
NP_573566.2:p.Ile1039Met
|
|