ENST00000269571.10:c.3492T>C
MANE Select
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ENSP00000269571.4:p.Gly1164=
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ENST00000269571.9:c.3492T>C
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ENSP00000269571.4:p.Gly1164=
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ENST00000406381.6:c.3402T>C
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ENSP00000385185.2:p.Gly1134=
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ENST00000445658.6:c.2664T>C
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ENSP00000404047.2:p.Gly888=
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ENST00000541774.5:c.3447T>C
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ENSP00000446466.1:p.Gly1149=
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ENST00000578373.5:c.*3282T>C
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ENSP00000463427.1:n.*3282T>C
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ENST00000584450.5:c.*71T>C
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ENSP00000463714.1:n.*71T>C
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ENST00000584601.5:c.3402T>C
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ENSP00000462438.1:p.Gly1134=
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NM_001005862.2:c.3402T>C , LRG_724t1:c.3402T>C
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NP_001005862.1:p.Gly1134=
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NM_001289936.1:c.3447T>C , LRG_724t4:c.3447T>C
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NP_001276865.1:p.Gly1149=
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NM_001289937.1:c.*71T>C
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NP_001276866.1:n.*71T>C
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NM_004448.3:c.3492T>C , LRG_724t2:c.3492T>C
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NP_004439.2:p.Gly1164=
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NR_110535.1:n.3816T>C
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XM_024450641.1:c.3630T>C
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XP_024306409.1:p.Gly1210=
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XM_024450642.1:c.3585T>C
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XP_024306410.1:p.Gly1195=
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XM_024450643.1:c.3540T>C
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XP_024306411.1:p.Gly1180=
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NM_001005862.3:c.3402T>C
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NP_001005862.1:p.Gly1134=
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NM_001289936.2:c.3447T>C
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NP_001276865.1:p.Gly1149=
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NM_001289937.2:c.*71T>C
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NP_001276866.1:n.*71T>C
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NM_001382782.1:c.3402T>C
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NP_001369711.1:p.Gly1134=
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NM_001382783.1:c.3402T>C
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NP_001369712.1:p.Gly1134=
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NM_001382784.1:c.3609T>C
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NP_001369713.1:p.Gly1203=
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NM_001382785.1:c.3594T>C
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NP_001369714.1:p.Gly1198=
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NM_001382786.1:c.3573T>C
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NP_001369715.1:p.Gly1191=
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NM_001382787.1:c.3567T>C
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NP_001369716.1:p.Gly1189=
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NM_001382788.1:c.3522T>C
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NP_001369717.1:p.Gly1174=
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NM_001382789.1:c.3513T>C
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NP_001369718.1:p.Gly1171=
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NM_001382790.1:c.3489T>C
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NP_001369719.1:p.Gly1163=
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NM_001382791.1:c.3483T>C
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NP_001369720.1:p.Gly1161=
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NM_001382792.1:c.3456T>C
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NP_001369721.1:p.Gly1152=
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NM_001382793.1:c.3450T>C
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NP_001369722.1:p.Gly1150=
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NM_001382794.1:c.3450T>C
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NP_001369723.1:p.Gly1150=
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NM_001382795.1:c.3444T>C
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NP_001369724.1:p.Gly1148=
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NM_001382796.1:c.3405T>C
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NP_001369725.1:p.Gly1135=
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NM_001382797.1:c.3393T>C
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NP_001369726.1:p.Gly1131=
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NM_001382798.1:c.3336T>C
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NP_001369727.1:p.Gly1112=
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NM_001382799.1:c.3312T>C
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NP_001369728.1:p.Gly1104=
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NM_001382800.1:c.3306T>C
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NP_001369729.1:p.Gly1102=
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NM_001382801.1:c.3288T>C
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NP_001369730.1:p.Gly1096=
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NM_001382802.1:c.3234T>C
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NP_001369731.1:p.Gly1078=
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NM_001382803.1:c.*71T>C
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NP_001369732.1:n.*71T>C
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NM_001382804.1:c.2664T>C
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NP_001369733.1:p.Gly888=
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NM_001382805.1:c.2541T>C
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NP_001369734.1:p.Gly847=
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NM_001382806.1:c.2454T>C
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NP_001369735.1:p.Gly818=
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NM_004448.4:c.3492T>C
MANE Select
|
NP_004439.2:p.Gly1164=
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NR_110535.2:n.3730T>C
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