ENST00000269571.10:c.3401G>C
MANE Select
|
ENSP00000269571.4:p.Ser1134Thr
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ENST00000269571.9:c.3401G>C
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ENSP00000269571.4:p.Ser1134Thr
|
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ENST00000406381.6:c.3311G>C
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ENSP00000385185.2:p.Ser1104Thr
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ENST00000445658.6:c.2573G>C
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ENSP00000404047.2:p.Ser858Thr
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ENST00000541774.5:c.3356G>C
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ENSP00000446466.1:p.Ser1119Thr
|
|
ENST00000578373.5:c.*3191G>C
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ENSP00000463427.1:n.*3191G>C
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ENST00000584450.5:c.3160-153G>C
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ENSP00000463714.1:n.3160-153G>C
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|
ENST00000584601.5:c.3311G>C
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ENSP00000462438.1:p.Ser1104Thr
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NM_001005862.2:c.3311G>C , LRG_724t1:c.3311G>C
|
NP_001005862.1:p.Ser1104Thr
|
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NM_001289936.1:c.3356G>C , LRG_724t4:c.3356G>C
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NP_001276865.1:p.Ser1119Thr
|
|
NM_001289937.1:c.3160-153G>C
|
NP_001276866.1:n.3160-153G>C
|
|
NM_004448.3:c.3401G>C , LRG_724t2:c.3401G>C
|
NP_004439.2:p.Ser1134Thr
|
|
NR_110535.1:n.3725G>C
|
|
|
XM_024450641.1:c.3539G>C
|
XP_024306409.1:p.Ser1180Thr
|
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XM_024450642.1:c.3494G>C
|
XP_024306410.1:p.Ser1165Thr
|
|
XM_024450643.1:c.3449G>C
|
XP_024306411.1:p.Ser1150Thr
|
|
NM_001005862.3:c.3311G>C
|
NP_001005862.1:p.Ser1104Thr
|
|
NM_001289936.2:c.3356G>C
|
NP_001276865.1:p.Ser1119Thr
|
|
NM_001289937.2:c.3160-153G>C
|
NP_001276866.1:n.3160-153G>C
|
|
NM_001382782.1:c.3311G>C
|
NP_001369711.1:p.Ser1104Thr
|
|
NM_001382783.1:c.3311G>C
|
NP_001369712.1:p.Ser1104Thr
|
|
NM_001382784.1:c.3518G>C
|
NP_001369713.1:p.Ser1173Thr
|
|
NM_001382785.1:c.3503G>C
|
NP_001369714.1:p.Ser1168Thr
|
|
NM_001382786.1:c.3482G>C
|
NP_001369715.1:p.Ser1161Thr
|
|
NM_001382787.1:c.3476G>C
|
NP_001369716.1:p.Ser1159Thr
|
|
NM_001382788.1:c.3431G>C
|
NP_001369717.1:p.Ser1144Thr
|
|
NM_001382789.1:c.3422G>C
|
NP_001369718.1:p.Ser1141Thr
|
|
NM_001382790.1:c.3398G>C
|
NP_001369719.1:p.Ser1133Thr
|
|
NM_001382791.1:c.3392G>C
|
NP_001369720.1:p.Ser1131Thr
|
|
NM_001382792.1:c.3365G>C
|
NP_001369721.1:p.Ser1122Thr
|
|
NM_001382793.1:c.3359G>C
|
NP_001369722.1:p.Ser1120Thr
|
|
NM_001382794.1:c.3359G>C
|
NP_001369723.1:p.Ser1120Thr
|
|
NM_001382795.1:c.3353G>C
|
NP_001369724.1:p.Ser1118Thr
|
|
NM_001382796.1:c.3314G>C
|
NP_001369725.1:p.Ser1105Thr
|
|
NM_001382797.1:c.3302G>C
|
NP_001369726.1:p.Ser1101Thr
|
|
NM_001382798.1:c.3245G>C
|
NP_001369727.1:p.Ser1082Thr
|
|
NM_001382799.1:c.3221G>C
|
NP_001369728.1:p.Ser1074Thr
|
|
NM_001382800.1:c.3215G>C
|
NP_001369729.1:p.Ser1072Thr
|
|
NM_001382801.1:c.3197G>C
|
NP_001369730.1:p.Ser1066Thr
|
|
NM_001382802.1:c.3143G>C
|
NP_001369731.1:p.Ser1048Thr
|
|
NM_001382803.1:c.3118-153G>C
|
NP_001369732.1:n.3118-153G>C
|
|
NM_001382804.1:c.2573G>C
|
NP_001369733.1:p.Ser858Thr
|
|
NM_001382805.1:c.2450G>C
|
NP_001369734.1:p.Ser817Thr
|
|
NM_001382806.1:c.2363G>C
|
NP_001369735.1:p.Ser788Thr
|
|
NM_004448.4:c.3401G>C
MANE Select
|
NP_004439.2:p.Ser1134Thr
|
|
NR_110535.2:n.3639G>C
|
|
|