ENST00000269571.10:c.3240G>T
MANE Select
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ENSP00000269571.4:p.Gly1080=
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ENST00000269571.9:c.3240G>T
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ENSP00000269571.4:p.Gly1080=
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ENST00000406381.6:c.3150G>T
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ENSP00000385185.2:p.Gly1050=
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ENST00000445658.6:c.2412G>T
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ENSP00000404047.2:p.Gly804=
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ENST00000541774.5:c.3195G>T
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ENSP00000446466.1:p.Gly1065=
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ENST00000578373.5:c.*3030G>T
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ENSP00000463427.1:n.*3030G>T
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ENST00000584450.5:c.3160-314G>T
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ENSP00000463714.1:n.3160-314G>T
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ENST00000584601.5:c.3150G>T
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ENSP00000462438.1:p.Gly1050=
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NM_001005862.2:c.3150G>T , LRG_724t1:c.3150G>T
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NP_001005862.1:p.Gly1050=
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NM_001289936.1:c.3195G>T , LRG_724t4:c.3195G>T
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NP_001276865.1:p.Gly1065=
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NM_001289937.1:c.3160-314G>T
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NP_001276866.1:n.3160-314G>T
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NM_004448.3:c.3240G>T , LRG_724t2:c.3240G>T
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NP_004439.2:p.Gly1080=
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NR_110535.1:n.3564G>T
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XM_024450641.1:c.3378G>T
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XP_024306409.1:p.Gly1126=
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XM_024450642.1:c.3333G>T
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XP_024306410.1:p.Gly1111=
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XM_024450643.1:c.3288G>T
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XP_024306411.1:p.Gly1096=
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NM_001005862.3:c.3150G>T
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NP_001005862.1:p.Gly1050=
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NM_001289936.2:c.3195G>T
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NP_001276865.1:p.Gly1065=
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NM_001289937.2:c.3160-314G>T
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NP_001276866.1:n.3160-314G>T
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NM_001382782.1:c.3150G>T
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NP_001369711.1:p.Gly1050=
|
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NM_001382783.1:c.3150G>T
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NP_001369712.1:p.Gly1050=
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NM_001382784.1:c.3357G>T
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NP_001369713.1:p.Gly1119=
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NM_001382785.1:c.3342G>T
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NP_001369714.1:p.Gly1114=
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NM_001382786.1:c.3321G>T
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NP_001369715.1:p.Gly1107=
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NM_001382787.1:c.3315G>T
|
NP_001369716.1:p.Gly1105=
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NM_001382788.1:c.3270G>T
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NP_001369717.1:p.Gly1090=
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NM_001382789.1:c.3261G>T
|
NP_001369718.1:p.Gly1087=
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NM_001382790.1:c.3237G>T
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NP_001369719.1:p.Gly1079=
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NM_001382791.1:c.3231G>T
|
NP_001369720.1:p.Gly1077=
|
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NM_001382792.1:c.3204G>T
|
NP_001369721.1:p.Gly1068=
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NM_001382793.1:c.3198G>T
|
NP_001369722.1:p.Gly1066=
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NM_001382794.1:c.3198G>T
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NP_001369723.1:p.Gly1066=
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NM_001382795.1:c.3192G>T
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NP_001369724.1:p.Gly1064=
|
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NM_001382796.1:c.3153G>T
|
NP_001369725.1:p.Gly1051=
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NM_001382797.1:c.3141G>T
|
NP_001369726.1:p.Gly1047=
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NM_001382798.1:c.3084G>T
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NP_001369727.1:p.Gly1028=
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NM_001382799.1:c.3060G>T
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NP_001369728.1:p.Gly1020=
|
|
NM_001382800.1:c.3054G>T
|
NP_001369729.1:p.Gly1018=
|
|
NM_001382801.1:c.3036G>T
|
NP_001369730.1:p.Gly1012=
|
|
NM_001382802.1:c.2982G>T
|
NP_001369731.1:p.Gly994=
|
|
NM_001382803.1:c.3118-314G>T
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NP_001369732.1:n.3118-314G>T
|
|
NM_001382804.1:c.2412G>T
|
NP_001369733.1:p.Gly804=
|
|
NM_001382805.1:c.2289G>T
|
NP_001369734.1:p.Gly763=
|
|
NM_001382806.1:c.2202G>T
|
NP_001369735.1:p.Gly734=
|
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NM_004448.4:c.3240G>T
MANE Select
|
NP_004439.2:p.Gly1080=
|
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NR_110535.2:n.3478G>T
|
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