ENST00000269571.10:c.3693G>C
MANE Select
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ENSP00000269571.4:p.Gly1231=
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ENST00000269571.9:c.3693G>C
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ENSP00000269571.4:p.Gly1231=
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ENST00000406381.6:c.3603G>C
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ENSP00000385185.2:p.Gly1201=
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ENST00000445658.6:c.2865G>C
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ENSP00000404047.2:p.Gly955=
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ENST00000541774.5:c.3648G>C
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ENSP00000446466.1:p.Gly1216=
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ENST00000578373.5:c.*3483G>C
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ENSP00000463427.1:n.*3483G>C
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ENST00000584450.5:c.*272G>C
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ENSP00000463714.1:n.*272G>C
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ENST00000584601.5:c.3603G>C
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ENSP00000462438.1:p.Gly1201=
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NM_001005862.2:c.3603G>C , LRG_724t1:c.3603G>C
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NP_001005862.1:p.Gly1201=
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NM_001289936.1:c.3648G>C , LRG_724t4:c.3648G>C
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NP_001276865.1:p.Gly1216=
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NM_001289937.1:c.*272G>C
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NP_001276866.1:n.*272G>C
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NM_004448.3:c.3693G>C , LRG_724t2:c.3693G>C
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NP_004439.2:p.Gly1231=
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NR_110535.1:n.4017G>C
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XM_024450641.1:c.3831G>C
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XP_024306409.1:p.Gly1277=
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XM_024450642.1:c.3786G>C
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XP_024306410.1:p.Gly1262=
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XM_024450643.1:c.3741G>C
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XP_024306411.1:p.Gly1247=
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NM_001005862.3:c.3603G>C
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NP_001005862.1:p.Gly1201=
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NM_001289936.2:c.3648G>C
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NP_001276865.1:p.Gly1216=
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NM_001289937.2:c.*272G>C
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NP_001276866.1:n.*272G>C
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NM_001382782.1:c.3603G>C
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NP_001369711.1:p.Gly1201=
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NM_001382783.1:c.3603G>C
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NP_001369712.1:p.Gly1201=
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NM_001382784.1:c.3810G>C
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NP_001369713.1:p.Gly1270=
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NM_001382785.1:c.3795G>C
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NP_001369714.1:p.Gly1265=
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NM_001382786.1:c.3774G>C
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NP_001369715.1:p.Gly1258=
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NM_001382787.1:c.3768G>C
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NP_001369716.1:p.Gly1256=
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NM_001382788.1:c.3723G>C
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NP_001369717.1:p.Gly1241=
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NM_001382789.1:c.3714G>C
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NP_001369718.1:p.Gly1238=
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NM_001382790.1:c.3690G>C
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NP_001369719.1:p.Gly1230=
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NM_001382791.1:c.3684G>C
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NP_001369720.1:p.Gly1228=
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NM_001382792.1:c.3657G>C
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NP_001369721.1:p.Gly1219=
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NM_001382793.1:c.3651G>C
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NP_001369722.1:p.Gly1217=
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NM_001382794.1:c.3651G>C
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NP_001369723.1:p.Gly1217=
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NM_001382795.1:c.3645G>C
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NP_001369724.1:p.Gly1215=
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NM_001382796.1:c.3606G>C
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NP_001369725.1:p.Gly1202=
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NM_001382797.1:c.3594G>C
|
NP_001369726.1:p.Gly1198=
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NM_001382798.1:c.3537G>C
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NP_001369727.1:p.Gly1179=
|
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NM_001382799.1:c.3513G>C
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NP_001369728.1:p.Gly1171=
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NM_001382800.1:c.3507G>C
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NP_001369729.1:p.Gly1169=
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NM_001382801.1:c.3489G>C
|
NP_001369730.1:p.Gly1163=
|
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NM_001382802.1:c.3435G>C
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NP_001369731.1:p.Gly1145=
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NM_001382803.1:c.*272G>C
|
NP_001369732.1:n.*272G>C
|
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NM_001382804.1:c.2865G>C
|
NP_001369733.1:p.Gly955=
|
|
NM_001382805.1:c.2742G>C
|
NP_001369734.1:p.Gly914=
|
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NM_001382806.1:c.2655G>C
|
NP_001369735.1:p.Gly885=
|
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NM_004448.4:c.3693G>C
MANE Select
|
NP_004439.2:p.Gly1231=
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NR_110535.2:n.3931G>C
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