ENST00000269571.10:c.3309A>G
MANE Select
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ENSP00000269571.4:p.Thr1103=
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ENST00000269571.9:c.3309A>G
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ENSP00000269571.4:p.Thr1103=
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ENST00000406381.6:c.3219A>G
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ENSP00000385185.2:p.Thr1073=
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ENST00000445658.6:c.2481A>G
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ENSP00000404047.2:p.Thr827=
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ENST00000541774.5:c.3264A>G
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ENSP00000446466.1:p.Thr1088=
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ENST00000578373.5:c.*3099A>G
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ENSP00000463427.1:n.*3099A>G
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ENST00000584450.5:c.3160-245A>G
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ENSP00000463714.1:n.3160-245A>G
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ENST00000584601.5:c.3219A>G
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ENSP00000462438.1:p.Thr1073=
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NM_001005862.2:c.3219A>G , LRG_724t1:c.3219A>G
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NP_001005862.1:p.Thr1073=
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NM_001289936.1:c.3264A>G , LRG_724t4:c.3264A>G
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NP_001276865.1:p.Thr1088=
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NM_001289937.1:c.3160-245A>G
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NP_001276866.1:n.3160-245A>G
|
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NM_004448.3:c.3309A>G , LRG_724t2:c.3309A>G
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NP_004439.2:p.Thr1103=
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NR_110535.1:n.3633A>G
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|
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XM_024450641.1:c.3447A>G
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XP_024306409.1:p.Thr1149=
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XM_024450642.1:c.3402A>G
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XP_024306410.1:p.Thr1134=
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XM_024450643.1:c.3357A>G
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XP_024306411.1:p.Thr1119=
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NM_001005862.3:c.3219A>G
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NP_001005862.1:p.Thr1073=
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NM_001289936.2:c.3264A>G
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NP_001276865.1:p.Thr1088=
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NM_001289937.2:c.3160-245A>G
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NP_001276866.1:n.3160-245A>G
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NM_001382782.1:c.3219A>G
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NP_001369711.1:p.Thr1073=
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NM_001382783.1:c.3219A>G
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NP_001369712.1:p.Thr1073=
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NM_001382784.1:c.3426A>G
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NP_001369713.1:p.Thr1142=
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NM_001382785.1:c.3411A>G
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NP_001369714.1:p.Thr1137=
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NM_001382786.1:c.3390A>G
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NP_001369715.1:p.Thr1130=
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NM_001382787.1:c.3384A>G
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NP_001369716.1:p.Thr1128=
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NM_001382788.1:c.3339A>G
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NP_001369717.1:p.Thr1113=
|
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NM_001382789.1:c.3330A>G
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NP_001369718.1:p.Thr1110=
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NM_001382790.1:c.3306A>G
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NP_001369719.1:p.Thr1102=
|
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NM_001382791.1:c.3300A>G
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NP_001369720.1:p.Thr1100=
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NM_001382792.1:c.3273A>G
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NP_001369721.1:p.Thr1091=
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NM_001382793.1:c.3267A>G
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NP_001369722.1:p.Thr1089=
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NM_001382794.1:c.3267A>G
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NP_001369723.1:p.Thr1089=
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NM_001382795.1:c.3261A>G
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NP_001369724.1:p.Thr1087=
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NM_001382796.1:c.3222A>G
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NP_001369725.1:p.Thr1074=
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NM_001382797.1:c.3210A>G
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NP_001369726.1:p.Thr1070=
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NM_001382798.1:c.3153A>G
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NP_001369727.1:p.Thr1051=
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NM_001382799.1:c.3129A>G
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NP_001369728.1:p.Thr1043=
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NM_001382800.1:c.3123A>G
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NP_001369729.1:p.Thr1041=
|
|
NM_001382801.1:c.3105A>G
|
NP_001369730.1:p.Thr1035=
|
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NM_001382802.1:c.3051A>G
|
NP_001369731.1:p.Thr1017=
|
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NM_001382803.1:c.3118-245A>G
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NP_001369732.1:n.3118-245A>G
|
|
NM_001382804.1:c.2481A>G
|
NP_001369733.1:p.Thr827=
|
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NM_001382805.1:c.2358A>G
|
NP_001369734.1:p.Thr786=
|
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NM_001382806.1:c.2271A>G
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NP_001369735.1:p.Thr757=
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NM_004448.4:c.3309A>G
MANE Select
|
NP_004439.2:p.Thr1103=
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NR_110535.2:n.3547A>G
|
|
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