ENST00000269571.10:c.3678C>G
MANE Select
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ENSP00000269571.4:p.Asp1226Glu
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ENST00000269571.9:c.3678C>G
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ENSP00000269571.4:p.Asp1226Glu
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ENST00000406381.6:c.3588C>G
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ENSP00000385185.2:p.Asp1196Glu
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ENST00000445658.6:c.2850C>G
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ENSP00000404047.2:p.Asp950Glu
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ENST00000541774.5:c.3633C>G
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ENSP00000446466.1:p.Asp1211Glu
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ENST00000578373.5:c.*3468C>G
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ENSP00000463427.1:n.*3468C>G
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ENST00000584450.5:c.*257C>G
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ENSP00000463714.1:n.*257C>G
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ENST00000584601.5:c.3588C>G
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ENSP00000462438.1:p.Asp1196Glu
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NM_001005862.2:c.3588C>G , LRG_724t1:c.3588C>G
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NP_001005862.1:p.Asp1196Glu
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NM_001289936.1:c.3633C>G , LRG_724t4:c.3633C>G
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NP_001276865.1:p.Asp1211Glu
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NM_001289937.1:c.*257C>G
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NP_001276866.1:n.*257C>G
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NM_004448.3:c.3678C>G , LRG_724t2:c.3678C>G
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NP_004439.2:p.Asp1226Glu
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NR_110535.1:n.4002C>G
|
|
|
XM_024450641.1:c.3816C>G
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XP_024306409.1:p.Asp1272Glu
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XM_024450642.1:c.3771C>G
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XP_024306410.1:p.Asp1257Glu
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XM_024450643.1:c.3726C>G
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XP_024306411.1:p.Asp1242Glu
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NM_001005862.3:c.3588C>G
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NP_001005862.1:p.Asp1196Glu
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|
NM_001289936.2:c.3633C>G
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NP_001276865.1:p.Asp1211Glu
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NM_001289937.2:c.*257C>G
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NP_001276866.1:n.*257C>G
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NM_001382782.1:c.3588C>G
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NP_001369711.1:p.Asp1196Glu
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NM_001382783.1:c.3588C>G
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NP_001369712.1:p.Asp1196Glu
|
|
NM_001382784.1:c.3795C>G
|
NP_001369713.1:p.Asp1265Glu
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|
NM_001382785.1:c.3780C>G
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NP_001369714.1:p.Asp1260Glu
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NM_001382786.1:c.3759C>G
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NP_001369715.1:p.Asp1253Glu
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NM_001382787.1:c.3753C>G
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NP_001369716.1:p.Asp1251Glu
|
|
NM_001382788.1:c.3708C>G
|
NP_001369717.1:p.Asp1236Glu
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|
NM_001382789.1:c.3699C>G
|
NP_001369718.1:p.Asp1233Glu
|
|
NM_001382790.1:c.3675C>G
|
NP_001369719.1:p.Asp1225Glu
|
|
NM_001382791.1:c.3669C>G
|
NP_001369720.1:p.Asp1223Glu
|
|
NM_001382792.1:c.3642C>G
|
NP_001369721.1:p.Asp1214Glu
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|
NM_001382793.1:c.3636C>G
|
NP_001369722.1:p.Asp1212Glu
|
|
NM_001382794.1:c.3636C>G
|
NP_001369723.1:p.Asp1212Glu
|
|
NM_001382795.1:c.3630C>G
|
NP_001369724.1:p.Asp1210Glu
|
|
NM_001382796.1:c.3591C>G
|
NP_001369725.1:p.Asp1197Glu
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|
NM_001382797.1:c.3579C>G
|
NP_001369726.1:p.Asp1193Glu
|
|
NM_001382798.1:c.3522C>G
|
NP_001369727.1:p.Asp1174Glu
|
|
NM_001382799.1:c.3498C>G
|
NP_001369728.1:p.Asp1166Glu
|
|
NM_001382800.1:c.3492C>G
|
NP_001369729.1:p.Asp1164Glu
|
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NM_001382801.1:c.3474C>G
|
NP_001369730.1:p.Asp1158Glu
|
|
NM_001382802.1:c.3420C>G
|
NP_001369731.1:p.Asp1140Glu
|
|
NM_001382803.1:c.*257C>G
|
NP_001369732.1:n.*257C>G
|
|
NM_001382804.1:c.2850C>G
|
NP_001369733.1:p.Asp950Glu
|
|
NM_001382805.1:c.2727C>G
|
NP_001369734.1:p.Asp909Glu
|
|
NM_001382806.1:c.2640C>G
|
NP_001369735.1:p.Asp880Glu
|
|
NM_004448.4:c.3678C>G
MANE Select
|
NP_004439.2:p.Asp1226Glu
|
|
NR_110535.2:n.3916C>G
|
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