ENST00000269571.10:c.3608C>G
MANE Select
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ENSP00000269571.4:p.Ala1203Gly
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ENST00000269571.9:c.3608C>G
|
ENSP00000269571.4:p.Ala1203Gly
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ENST00000406381.6:c.3518C>G
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ENSP00000385185.2:p.Ala1173Gly
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ENST00000445658.6:c.2780C>G
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ENSP00000404047.2:p.Ala927Gly
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ENST00000541774.5:c.3563C>G
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ENSP00000446466.1:p.Ala1188Gly
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ENST00000578373.5:c.*3398C>G
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ENSP00000463427.1:n.*3398C>G
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ENST00000584450.5:c.*187C>G
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ENSP00000463714.1:n.*187C>G
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ENST00000584601.5:c.3518C>G
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ENSP00000462438.1:p.Ala1173Gly
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NM_001005862.2:c.3518C>G , LRG_724t1:c.3518C>G
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NP_001005862.1:p.Ala1173Gly
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NM_001289936.1:c.3563C>G , LRG_724t4:c.3563C>G
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NP_001276865.1:p.Ala1188Gly
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NM_001289937.1:c.*187C>G
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NP_001276866.1:n.*187C>G
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NM_004448.3:c.3608C>G , LRG_724t2:c.3608C>G
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NP_004439.2:p.Ala1203Gly
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NR_110535.1:n.3932C>G
|
|
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XM_024450641.1:c.3746C>G
|
XP_024306409.1:p.Ala1249Gly
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XM_024450642.1:c.3701C>G
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XP_024306410.1:p.Ala1234Gly
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XM_024450643.1:c.3656C>G
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XP_024306411.1:p.Ala1219Gly
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NM_001005862.3:c.3518C>G
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NP_001005862.1:p.Ala1173Gly
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NM_001289936.2:c.3563C>G
|
NP_001276865.1:p.Ala1188Gly
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NM_001289937.2:c.*187C>G
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NP_001276866.1:n.*187C>G
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NM_001382782.1:c.3518C>G
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NP_001369711.1:p.Ala1173Gly
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NM_001382783.1:c.3518C>G
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NP_001369712.1:p.Ala1173Gly
|
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NM_001382784.1:c.3725C>G
|
NP_001369713.1:p.Ala1242Gly
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NM_001382785.1:c.3710C>G
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NP_001369714.1:p.Ala1237Gly
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NM_001382786.1:c.3689C>G
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NP_001369715.1:p.Ala1230Gly
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NM_001382787.1:c.3683C>G
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NP_001369716.1:p.Ala1228Gly
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NM_001382788.1:c.3638C>G
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NP_001369717.1:p.Ala1213Gly
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NM_001382789.1:c.3629C>G
|
NP_001369718.1:p.Ala1210Gly
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NM_001382790.1:c.3605C>G
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NP_001369719.1:p.Ala1202Gly
|
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NM_001382791.1:c.3599C>G
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NP_001369720.1:p.Ala1200Gly
|
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NM_001382792.1:c.3572C>G
|
NP_001369721.1:p.Ala1191Gly
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NM_001382793.1:c.3566C>G
|
NP_001369722.1:p.Ala1189Gly
|
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NM_001382794.1:c.3566C>G
|
NP_001369723.1:p.Ala1189Gly
|
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NM_001382795.1:c.3560C>G
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NP_001369724.1:p.Ala1187Gly
|
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NM_001382796.1:c.3521C>G
|
NP_001369725.1:p.Ala1174Gly
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NM_001382797.1:c.3509C>G
|
NP_001369726.1:p.Ala1170Gly
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NM_001382798.1:c.3452C>G
|
NP_001369727.1:p.Ala1151Gly
|
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NM_001382799.1:c.3428C>G
|
NP_001369728.1:p.Ala1143Gly
|
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NM_001382800.1:c.3422C>G
|
NP_001369729.1:p.Ala1141Gly
|
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NM_001382801.1:c.3404C>G
|
NP_001369730.1:p.Ala1135Gly
|
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NM_001382802.1:c.3350C>G
|
NP_001369731.1:p.Ala1117Gly
|
|
NM_001382803.1:c.*187C>G
|
NP_001369732.1:n.*187C>G
|
|
NM_001382804.1:c.2780C>G
|
NP_001369733.1:p.Ala927Gly
|
|
NM_001382805.1:c.2657C>G
|
NP_001369734.1:p.Ala886Gly
|
|
NM_001382806.1:c.2570C>G
|
NP_001369735.1:p.Ala857Gly
|
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NM_004448.4:c.3608C>G
MANE Select
|
NP_004439.2:p.Ala1203Gly
|
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NR_110535.2:n.3846C>G
|
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