ENST00000269571.10:c.3250G>T
MANE Select
|
ENSP00000269571.4:p.Asp1084Tyr
|
|
ENST00000269571.9:c.3250G>T
|
ENSP00000269571.4:p.Asp1084Tyr
|
|
ENST00000406381.6:c.3160G>T
|
ENSP00000385185.2:p.Asp1054Tyr
|
|
ENST00000445658.6:c.2422G>T
|
ENSP00000404047.2:p.Asp808Tyr
|
|
ENST00000541774.5:c.3205G>T
|
ENSP00000446466.1:p.Asp1069Tyr
|
|
ENST00000578373.5:c.*3040G>T
|
ENSP00000463427.1:n.*3040G>T
|
|
ENST00000584450.5:c.3160-304G>T
|
ENSP00000463714.1:n.3160-304G>T
|
|
ENST00000584601.5:c.3160G>T
|
ENSP00000462438.1:p.Asp1054Tyr
|
|
NM_001005862.2:c.3160G>T , LRG_724t1:c.3160G>T
|
NP_001005862.1:p.Asp1054Tyr
|
|
NM_001289936.1:c.3205G>T , LRG_724t4:c.3205G>T
|
NP_001276865.1:p.Asp1069Tyr
|
|
NM_001289937.1:c.3160-304G>T
|
NP_001276866.1:n.3160-304G>T
|
|
NM_004448.3:c.3250G>T , LRG_724t2:c.3250G>T
|
NP_004439.2:p.Asp1084Tyr
|
|
NR_110535.1:n.3574G>T
|
|
|
XM_024450641.1:c.3388G>T
|
XP_024306409.1:p.Asp1130Tyr
|
|
XM_024450642.1:c.3343G>T
|
XP_024306410.1:p.Asp1115Tyr
|
|
XM_024450643.1:c.3298G>T
|
XP_024306411.1:p.Asp1100Tyr
|
|
NM_001005862.3:c.3160G>T
|
NP_001005862.1:p.Asp1054Tyr
|
|
NM_001289936.2:c.3205G>T
|
NP_001276865.1:p.Asp1069Tyr
|
|
NM_001289937.2:c.3160-304G>T
|
NP_001276866.1:n.3160-304G>T
|
|
NM_001382782.1:c.3160G>T
|
NP_001369711.1:p.Asp1054Tyr
|
|
NM_001382783.1:c.3160G>T
|
NP_001369712.1:p.Asp1054Tyr
|
|
NM_001382784.1:c.3367G>T
|
NP_001369713.1:p.Asp1123Tyr
|
|
NM_001382785.1:c.3352G>T
|
NP_001369714.1:p.Asp1118Tyr
|
|
NM_001382786.1:c.3331G>T
|
NP_001369715.1:p.Asp1111Tyr
|
|
NM_001382787.1:c.3325G>T
|
NP_001369716.1:p.Asp1109Tyr
|
|
NM_001382788.1:c.3280G>T
|
NP_001369717.1:p.Asp1094Tyr
|
|
NM_001382789.1:c.3271G>T
|
NP_001369718.1:p.Asp1091Tyr
|
|
NM_001382790.1:c.3247G>T
|
NP_001369719.1:p.Asp1083Tyr
|
|
NM_001382791.1:c.3241G>T
|
NP_001369720.1:p.Asp1081Tyr
|
|
NM_001382792.1:c.3214G>T
|
NP_001369721.1:p.Asp1072Tyr
|
|
NM_001382793.1:c.3208G>T
|
NP_001369722.1:p.Asp1070Tyr
|
|
NM_001382794.1:c.3208G>T
|
NP_001369723.1:p.Asp1070Tyr
|
|
NM_001382795.1:c.3202G>T
|
NP_001369724.1:p.Asp1068Tyr
|
|
NM_001382796.1:c.3163G>T
|
NP_001369725.1:p.Asp1055Tyr
|
|
NM_001382797.1:c.3151G>T
|
NP_001369726.1:p.Asp1051Tyr
|
|
NM_001382798.1:c.3094G>T
|
NP_001369727.1:p.Asp1032Tyr
|
|
NM_001382799.1:c.3070G>T
|
NP_001369728.1:p.Asp1024Tyr
|
|
NM_001382800.1:c.3064G>T
|
NP_001369729.1:p.Asp1022Tyr
|
|
NM_001382801.1:c.3046G>T
|
NP_001369730.1:p.Asp1016Tyr
|
|
NM_001382802.1:c.2992G>T
|
NP_001369731.1:p.Asp998Tyr
|
|
NM_001382803.1:c.3118-304G>T
|
NP_001369732.1:n.3118-304G>T
|
|
NM_001382804.1:c.2422G>T
|
NP_001369733.1:p.Asp808Tyr
|
|
NM_001382805.1:c.2299G>T
|
NP_001369734.1:p.Asp767Tyr
|
|
NM_001382806.1:c.2212G>T
|
NP_001369735.1:p.Asp738Tyr
|
|
NM_004448.4:c.3250G>T
MANE Select
|
NP_004439.2:p.Asp1084Tyr
|
|
NR_110535.2:n.3488G>T
|
|
|