ENST00000376131.9:c.466G>C
|
ENSP00000365301.3:p.Glu156Gln
|
|
ENST00000418923.3:c.349G>C
|
ENSP00000516414.1:p.Glu117Gln
|
|
ENST00000706491.1:c.*55G>C
|
ENSP00000516413.1:n.*55G>C
|
|
ENST00000706492.1:c.*270G>C
|
ENSP00000516415.1:n.*270G>C
|
|
ENST00000706493.1:c.*365G>C
|
ENSP00000516416.1:n.*365G>C
|
|
ENST00000706494.1:c.199G>C
|
ENSP00000516417.1:p.Glu67Gln
|
|
ENST00000376143.5:c.451G>C
MANE Select
|
ENSP00000365313.4:p.Glu151Gln
|
|
ENST00000376131.8:c.466G>C
|
ENSP00000365301.3:p.Glu156Gln
|
|
ENST00000376143.4:c.451G>C
|
ENSP00000365313.4:p.Glu151Gln
|
|
NM_004115.3:c.451G>C
|
NP_004106.1:p.Glu151Gln
|
|
NM_175929.2:c.466G>C
|
NP_787125.1:p.Glu156Gln
|
|
XM_011521053.1:c.271G>C
|
XP_011519355.1:p.Glu91Gln
|
|
NM_001321931.1:c.199G>C
|
NP_001308860.1:p.Glu67Gln
|
|
NM_001321932.1:c.262G>C
|
NP_001308861.1:p.Glu88Gln
|
|
NM_001321933.1:c.271G>C
|
NP_001308862.1:p.Glu91Gln
|
|
NM_001321934.1:c.199G>C
|
NP_001308863.1:p.Glu67Gln
|
|
NM_001321935.1:c.199G>C
|
NP_001308864.1:p.Glu67Gln
|
|
NM_001321936.1:c.262G>C
|
NP_001308865.1:p.Glu88Gln
|
|
NM_001321938.1:c.271G>C
|
NP_001308867.1:p.Glu91Gln
|
|
NM_001321939.1:c.355G>C
|
NP_001308868.1:p.Glu119Gln
|
|
NM_001321940.1:c.271G>C
|
NP_001308869.1:p.Glu91Gln
|
|
NM_001321941.1:c.265G>C
|
NP_001308870.1:p.Glu89Gln
|
|
NM_001321942.1:c.199G>C
|
NP_001308871.1:p.Glu67Gln
|
|
NM_001321943.1:c.199G>C
|
NP_001308872.1:p.Glu67Gln
|
|
NM_001321944.1:c.262G>C
|
NP_001308873.1:p.Glu88Gln
|
|
NM_001321945.1:c.349G>C
|
NP_001308874.1:p.Glu117Gln
|
|
NM_001321946.1:c.199G>C
|
NP_001308875.1:p.Glu67Gln
|
|
NM_001321947.1:c.310G>C
|
NP_001308876.1:p.Glu104Gln
|
|
NM_001321948.1:c.349G>C
|
NP_001308877.1:p.Glu117Gln
|
|
NM_001321949.1:c.199G>C
|
NP_001308878.1:p.Glu67Gln
|
|
NM_001321938.2:c.271G>C
|
NP_001308867.1:p.Glu91Gln
|
|
NM_001321945.2:c.349G>C
|
NP_001308874.1:p.Glu117Gln
|
|
NM_001321946.2:c.199G>C
|
NP_001308875.1:p.Glu67Gln
|
|
NM_001321947.2:c.310G>C
|
NP_001308876.1:p.Glu104Gln
|
|
NM_001321948.2:c.349G>C
|
NP_001308877.1:p.Glu117Gln
|
|
NM_001321939.2:c.355G>C
|
NP_001308868.1:p.Glu119Gln
|
|
NM_001321941.2:c.265G>C
|
NP_001308870.1:p.Glu89Gln
|
|
NM_001379342.1:c.349G>C
|
NP_001366271.1:p.Glu117Gln
|
|
NM_004115.4:c.451G>C
MANE Select
|
NP_004106.1:p.Glu151Gln
|
|
NM_175929.3:c.466G>C
|
NP_787125.1:p.Glu156Gln
|
|