ENST00000376131.9:c.575T>C
|
ENSP00000365301.3:p.Val192Ala
|
|
ENST00000418923.3:c.458T>C
|
ENSP00000516414.1:p.Val153Ala
|
|
ENST00000706491.1:c.*164T>C
|
ENSP00000516413.1:n.*164T>C
|
|
ENST00000706492.1:c.*379T>C
|
ENSP00000516415.1:n.*379T>C
|
|
ENST00000706493.1:c.*474T>C
|
ENSP00000516416.1:n.*474T>C
|
|
ENST00000706494.1:c.308T>C
|
ENSP00000516417.1:p.Val103Ala
|
|
ENST00000376143.5:c.560T>C
MANE Select
|
ENSP00000365313.4:p.Val187Ala
|
|
ENST00000376131.8:c.575T>C
|
ENSP00000365301.3:p.Val192Ala
|
|
ENST00000376143.4:c.560T>C
|
ENSP00000365313.4:p.Val187Ala
|
|
NM_004115.3:c.560T>C
|
NP_004106.1:p.Val187Ala
|
|
NM_175929.2:c.575T>C
|
NP_787125.1:p.Val192Ala
|
|
XM_011521053.1:c.380T>C
|
XP_011519355.1:p.Val127Ala
|
|
NM_001321931.1:c.308T>C
|
NP_001308860.1:p.Val103Ala
|
|
NM_001321932.1:c.371T>C
|
NP_001308861.1:p.Val124Ala
|
|
NM_001321933.1:c.380T>C
|
NP_001308862.1:p.Val127Ala
|
|
NM_001321934.1:c.308T>C
|
NP_001308863.1:p.Val103Ala
|
|
NM_001321935.1:c.308T>C
|
NP_001308864.1:p.Val103Ala
|
|
NM_001321936.1:c.371T>C
|
NP_001308865.1:p.Val124Ala
|
|
NM_001321938.1:c.380T>C
|
NP_001308867.1:p.Val127Ala
|
|
NM_001321939.1:c.464T>C
|
NP_001308868.1:p.Val155Ala
|
|
NM_001321940.1:c.380T>C
|
NP_001308869.1:p.Val127Ala
|
|
NM_001321941.1:c.374T>C
|
NP_001308870.1:p.Val125Ala
|
|
NM_001321942.1:c.308T>C
|
NP_001308871.1:p.Val103Ala
|
|
NM_001321943.1:c.308T>C
|
NP_001308872.1:p.Val103Ala
|
|
NM_001321944.1:c.371T>C
|
NP_001308873.1:p.Val124Ala
|
|
NM_001321945.1:c.458T>C
|
NP_001308874.1:p.Val153Ala
|
|
NM_001321946.1:c.308T>C
|
NP_001308875.1:p.Val103Ala
|
|
NM_001321947.1:c.419T>C
|
NP_001308876.1:p.Val140Ala
|
|
NM_001321948.1:c.458T>C
|
NP_001308877.1:p.Val153Ala
|
|
NM_001321949.1:c.308T>C
|
NP_001308878.1:p.Val103Ala
|
|
NM_001321938.2:c.380T>C
|
NP_001308867.1:p.Val127Ala
|
|
NM_001321945.2:c.458T>C
|
NP_001308874.1:p.Val153Ala
|
|
NM_001321946.2:c.308T>C
|
NP_001308875.1:p.Val103Ala
|
|
NM_001321947.2:c.419T>C
|
NP_001308876.1:p.Val140Ala
|
|
NM_001321948.2:c.458T>C
|
NP_001308877.1:p.Val153Ala
|
|
NM_001321939.2:c.464T>C
|
NP_001308868.1:p.Val155Ala
|
|
NM_001321941.2:c.374T>C
|
NP_001308870.1:p.Val125Ala
|
|
NM_001379342.1:c.458T>C
|
NP_001366271.1:p.Val153Ala
|
|
NM_004115.4:c.560T>C
MANE Select
|
NP_004106.1:p.Val187Ala
|
|
NM_175929.3:c.575T>C
|
NP_787125.1:p.Val192Ala
|
|