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ENST00000269571.10:c.3196T>G
MANE Select
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ENSP00000269571.4:p.Ser1066Ala
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ENST00000269571.9:c.3196T>G
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ENSP00000269571.4:p.Ser1066Ala
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ENST00000406381.6:c.3106T>G
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ENSP00000385185.2:p.Ser1036Ala
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ENST00000445658.6:c.2368T>G
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ENSP00000404047.2:p.Ser790Ala
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ENST00000541774.5:c.3151T>G
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ENSP00000446466.1:p.Ser1051Ala
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ENST00000578373.5:c.*2986T>G
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ENSP00000463427.1:n.*2986T>G
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ENST00000584450.5:c.3159+328T>G
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ENSP00000463714.1:n.3159+328T>G
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ENST00000584601.5:c.3106T>G
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ENSP00000462438.1:p.Ser1036Ala
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NM_001005862.2:c.3106T>G , LRG_724t1:c.3106T>G
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NP_001005862.1:p.Ser1036Ala
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NM_001289936.1:c.3151T>G , LRG_724t4:c.3151T>G
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NP_001276865.1:p.Ser1051Ala
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NM_001289937.1:c.3159+328T>G
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NP_001276866.1:n.3159+328T>G
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NM_004448.3:c.3196T>G , LRG_724t2:c.3196T>G
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NP_004439.2:p.Ser1066Ala
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NR_110535.1:n.3520T>G
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XM_024450641.1:c.3334T>G
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XP_024306409.1:p.Ser1112Ala
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XM_024450642.1:c.3289T>G
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XP_024306410.1:p.Ser1097Ala
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XM_024450643.1:c.3244T>G
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XP_024306411.1:p.Ser1082Ala
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NM_001005862.3:c.3106T>G
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NP_001005862.1:p.Ser1036Ala
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NM_001289936.2:c.3151T>G
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NP_001276865.1:p.Ser1051Ala
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NM_001289937.2:c.3159+328T>G
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NP_001276866.1:n.3159+328T>G
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NM_001382782.1:c.3106T>G
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NP_001369711.1:p.Ser1036Ala
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NM_001382783.1:c.3106T>G
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NP_001369712.1:p.Ser1036Ala
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NM_001382784.1:c.3313T>G
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NP_001369713.1:p.Ser1105Ala
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NM_001382785.1:c.3298T>G
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NP_001369714.1:p.Ser1100Ala
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NM_001382786.1:c.3277T>G
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NP_001369715.1:p.Ser1093Ala
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NM_001382787.1:c.3271T>G
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NP_001369716.1:p.Ser1091Ala
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NM_001382788.1:c.3226T>G
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NP_001369717.1:p.Ser1076Ala
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NM_001382789.1:c.3217T>G
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NP_001369718.1:p.Ser1073Ala
|
|
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NM_001382790.1:c.3193T>G
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NP_001369719.1:p.Ser1065Ala
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NM_001382791.1:c.3187T>G
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NP_001369720.1:p.Ser1063Ala
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|
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NM_001382792.1:c.3160T>G
|
NP_001369721.1:p.Ser1054Ala
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NM_001382793.1:c.3154T>G
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NP_001369722.1:p.Ser1052Ala
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NM_001382794.1:c.3154T>G
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NP_001369723.1:p.Ser1052Ala
|
|
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NM_001382795.1:c.3148T>G
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NP_001369724.1:p.Ser1050Ala
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NM_001382796.1:c.3109T>G
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NP_001369725.1:p.Ser1037Ala
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NM_001382797.1:c.3097T>G
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NP_001369726.1:p.Ser1033Ala
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NM_001382798.1:c.3040T>G
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NP_001369727.1:p.Ser1014Ala
|
|
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NM_001382799.1:c.3016T>G
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NP_001369728.1:p.Ser1006Ala
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|
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NM_001382800.1:c.3010T>G
|
NP_001369729.1:p.Ser1004Ala
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|
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NM_001382801.1:c.2992T>G
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NP_001369730.1:p.Ser998Ala
|
|
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NM_001382802.1:c.2938T>G
|
NP_001369731.1:p.Ser980Ala
|
|
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NM_001382803.1:c.3117+328T>G
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NP_001369732.1:n.3117+328T>G
|
|
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NM_001382804.1:c.2368T>G
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NP_001369733.1:p.Ser790Ala
|
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NM_001382805.1:c.2245T>G
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NP_001369734.1:p.Ser749Ala
|
|
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NM_001382806.1:c.2158T>G
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NP_001369735.1:p.Ser720Ala
|
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NM_004448.4:c.3196T>G
MANE Select
|
NP_004439.2:p.Ser1066Ala
|
|
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NR_110535.2:n.3434T>G
|
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