ENST00000376131.9:c.476A>C
|
ENSP00000365301.3:p.Tyr159Ser
|
|
ENST00000418923.3:c.359A>C
|
ENSP00000516414.1:p.Tyr120Ser
|
|
ENST00000706491.1:c.*65A>C
|
ENSP00000516413.1:n.*65A>C
|
|
ENST00000706492.1:c.*280A>C
|
ENSP00000516415.1:n.*280A>C
|
|
ENST00000706493.1:c.*375A>C
|
ENSP00000516416.1:n.*375A>C
|
|
ENST00000706494.1:c.209A>C
|
ENSP00000516417.1:p.Tyr70Ser
|
|
ENST00000376143.5:c.461A>C
MANE Select
|
ENSP00000365313.4:p.Tyr154Ser
|
|
ENST00000376131.8:c.476A>C
|
ENSP00000365301.3:p.Tyr159Ser
|
|
ENST00000376143.4:c.461A>C
|
ENSP00000365313.4:p.Tyr154Ser
|
|
NM_004115.3:c.461A>C
|
NP_004106.1:p.Tyr154Ser
|
|
NM_175929.2:c.476A>C
|
NP_787125.1:p.Tyr159Ser
|
|
XM_011521053.1:c.281A>C
|
XP_011519355.1:p.Tyr94Ser
|
|
NM_001321931.1:c.209A>C
|
NP_001308860.1:p.Tyr70Ser
|
|
NM_001321932.1:c.272A>C
|
NP_001308861.1:p.Tyr91Ser
|
|
NM_001321933.1:c.281A>C
|
NP_001308862.1:p.Tyr94Ser
|
|
NM_001321934.1:c.209A>C
|
NP_001308863.1:p.Tyr70Ser
|
|
NM_001321935.1:c.209A>C
|
NP_001308864.1:p.Tyr70Ser
|
|
NM_001321936.1:c.272A>C
|
NP_001308865.1:p.Tyr91Ser
|
|
NM_001321938.1:c.281A>C
|
NP_001308867.1:p.Tyr94Ser
|
|
NM_001321939.1:c.365A>C
|
NP_001308868.1:p.Tyr122Ser
|
|
NM_001321940.1:c.281A>C
|
NP_001308869.1:p.Tyr94Ser
|
|
NM_001321941.1:c.275A>C
|
NP_001308870.1:p.Tyr92Ser
|
|
NM_001321942.1:c.209A>C
|
NP_001308871.1:p.Tyr70Ser
|
|
NM_001321943.1:c.209A>C
|
NP_001308872.1:p.Tyr70Ser
|
|
NM_001321944.1:c.272A>C
|
NP_001308873.1:p.Tyr91Ser
|
|
NM_001321945.1:c.359A>C
|
NP_001308874.1:p.Tyr120Ser
|
|
NM_001321946.1:c.209A>C
|
NP_001308875.1:p.Tyr70Ser
|
|
NM_001321947.1:c.320A>C
|
NP_001308876.1:p.Tyr107Ser
|
|
NM_001321948.1:c.359A>C
|
NP_001308877.1:p.Tyr120Ser
|
|
NM_001321949.1:c.209A>C
|
NP_001308878.1:p.Tyr70Ser
|
|
NM_001321938.2:c.281A>C
|
NP_001308867.1:p.Tyr94Ser
|
|
NM_001321945.2:c.359A>C
|
NP_001308874.1:p.Tyr120Ser
|
|
NM_001321946.2:c.209A>C
|
NP_001308875.1:p.Tyr70Ser
|
|
NM_001321947.2:c.320A>C
|
NP_001308876.1:p.Tyr107Ser
|
|
NM_001321948.2:c.359A>C
|
NP_001308877.1:p.Tyr120Ser
|
|
NM_001321939.2:c.365A>C
|
NP_001308868.1:p.Tyr122Ser
|
|
NM_001321941.2:c.275A>C
|
NP_001308870.1:p.Tyr92Ser
|
|
NM_001379342.1:c.359A>C
|
NP_001366271.1:p.Tyr120Ser
|
|
NM_004115.4:c.461A>C
MANE Select
|
NP_004106.1:p.Tyr154Ser
|
|
NM_175929.3:c.476A>C
|
NP_787125.1:p.Tyr159Ser
|
|