ENST00000357578.8:c.1263G>T
MANE Select
|
ENSP00000350191.3:p.Glu421Asp
|
|
ENST00000479394.2:n.378G>T
|
|
|
ENST00000672352.1:c.882G>T
|
ENSP00000500876.1:p.Glu294Asp
|
|
ENST00000672652.1:c.1226G>T
|
|
|
ENST00000348925.2:c.1302G>T
|
ENSP00000314649.3:p.Glu434Asp
|
|
ENST00000357578.7:c.1263G>T
|
ENSP00000350191.3:p.Glu421Asp
|
|
ENST00000479394.1:n.378G>T
|
|
|
ENST00000491546.5:c.1179G>T
|
ENSP00000417687.1:p.Glu393Asp
|
|
NM_001080.3:c.1263G>T
MANE Select
|
NP_001071.1:p.Glu421Asp
|
|
NM_170740.1:c.1302G>T
|
NP_733936.1:p.Glu434Asp
|
|
NM_001368954.1:c.1119G>T
|
NP_001355883.1:p.Glu373Asp
|
|