ENST00000376131.9:c.503G>T
|
ENSP00000365301.3:p.Arg168Ile
|
|
ENST00000418923.3:c.386G>T
|
ENSP00000516414.1:p.Arg129Ile
|
|
ENST00000706491.1:c.*92G>T
|
ENSP00000516413.1:n.*92G>T
|
|
ENST00000706492.1:c.*307G>T
|
ENSP00000516415.1:n.*307G>T
|
|
ENST00000706493.1:c.*402G>T
|
ENSP00000516416.1:n.*402G>T
|
|
ENST00000706494.1:c.236G>T
|
ENSP00000516417.1:p.Arg79Ile
|
|
ENST00000376143.5:c.488G>T
MANE Select
|
ENSP00000365313.4:p.Arg163Ile
|
|
ENST00000376131.8:c.503G>T
|
ENSP00000365301.3:p.Arg168Ile
|
|
ENST00000376143.4:c.488G>T
|
ENSP00000365313.4:p.Arg163Ile
|
|
NM_004115.3:c.488G>T
|
NP_004106.1:p.Arg163Ile
|
|
NM_175929.2:c.503G>T
|
NP_787125.1:p.Arg168Ile
|
|
XM_011521053.1:c.308G>T
|
XP_011519355.1:p.Arg103Ile
|
|
NM_001321931.1:c.236G>T
|
NP_001308860.1:p.Arg79Ile
|
|
NM_001321932.1:c.299G>T
|
NP_001308861.1:p.Arg100Ile
|
|
NM_001321933.1:c.308G>T
|
NP_001308862.1:p.Arg103Ile
|
|
NM_001321934.1:c.236G>T
|
NP_001308863.1:p.Arg79Ile
|
|
NM_001321935.1:c.236G>T
|
NP_001308864.1:p.Arg79Ile
|
|
NM_001321936.1:c.299G>T
|
NP_001308865.1:p.Arg100Ile
|
|
NM_001321938.1:c.308G>T
|
NP_001308867.1:p.Arg103Ile
|
|
NM_001321939.1:c.392G>T
|
NP_001308868.1:p.Arg131Ile
|
|
NM_001321940.1:c.308G>T
|
NP_001308869.1:p.Arg103Ile
|
|
NM_001321941.1:c.302G>T
|
NP_001308870.1:p.Arg101Ile
|
|
NM_001321942.1:c.236G>T
|
NP_001308871.1:p.Arg79Ile
|
|
NM_001321943.1:c.236G>T
|
NP_001308872.1:p.Arg79Ile
|
|
NM_001321944.1:c.299G>T
|
NP_001308873.1:p.Arg100Ile
|
|
NM_001321945.1:c.386G>T
|
NP_001308874.1:p.Arg129Ile
|
|
NM_001321946.1:c.236G>T
|
NP_001308875.1:p.Arg79Ile
|
|
NM_001321947.1:c.347G>T
|
NP_001308876.1:p.Arg116Ile
|
|
NM_001321948.1:c.386G>T
|
NP_001308877.1:p.Arg129Ile
|
|
NM_001321949.1:c.236G>T
|
NP_001308878.1:p.Arg79Ile
|
|
NM_001321938.2:c.308G>T
|
NP_001308867.1:p.Arg103Ile
|
|
NM_001321945.2:c.386G>T
|
NP_001308874.1:p.Arg129Ile
|
|
NM_001321946.2:c.236G>T
|
NP_001308875.1:p.Arg79Ile
|
|
NM_001321947.2:c.347G>T
|
NP_001308876.1:p.Arg116Ile
|
|
NM_001321948.2:c.386G>T
|
NP_001308877.1:p.Arg129Ile
|
|
NM_001321939.2:c.392G>T
|
NP_001308868.1:p.Arg131Ile
|
|
NM_001321941.2:c.302G>T
|
NP_001308870.1:p.Arg101Ile
|
|
NM_001379342.1:c.386G>T
|
NP_001366271.1:p.Arg129Ile
|
|
NM_004115.4:c.488G>T
MANE Select
|
NP_004106.1:p.Arg163Ile
|
|
NM_175929.3:c.503G>T
|
NP_787125.1:p.Arg168Ile
|
|