ENST00000357578.8:c.553G>T
MANE Select
|
ENSP00000350191.3:p.Asp185Tyr
|
|
ENST00000672352.1:c.316G>T
|
ENSP00000500876.1:p.Asp106Tyr
|
|
ENST00000672557.1:c.471G>T
|
|
|
ENST00000672652.1:c.474G>T
|
|
|
ENST00000675422.1:n.1313G>T
|
|
|
ENST00000348925.2:c.553G>T
|
ENSP00000314649.3:p.Asp185Tyr
|
|
ENST00000357578.7:c.553G>T
|
ENSP00000350191.3:p.Asp185Tyr
|
|
ENST00000491546.5:c.469G>T
|
ENSP00000417687.1:p.Asp157Tyr
|
|
NM_001080.3:c.553G>T
MANE Select
|
NP_001071.1:p.Asp185Tyr
|
|
NM_170740.1:c.553G>T
|
NP_733936.1:p.Asp185Tyr
|
|
NM_001368954.1:c.553G>T
|
NP_001355883.1:p.Asp185Tyr
|
|