ENST00000357578.8:c.1199T>G
MANE Select
|
ENSP00000350191.3:p.Val400Gly
|
|
ENST00000479394.2:n.314T>G
|
|
|
ENST00000672352.1:c.818T>G
|
ENSP00000500876.1:p.Val273Gly
|
|
ENST00000672652.1:c.1162T>G
|
|
|
ENST00000348925.2:c.1238T>G
|
ENSP00000314649.3:p.Val413Gly
|
|
ENST00000357578.7:c.1199T>G
|
ENSP00000350191.3:p.Val400Gly
|
|
ENST00000479394.1:n.314T>G
|
|
|
ENST00000491546.5:c.1115T>G
|
ENSP00000417687.1:p.Val372Gly
|
|
NM_001080.3:c.1199T>G
MANE Select
|
NP_001071.1:p.Val400Gly
|
|
NM_170740.1:c.1238T>G
|
NP_733936.1:p.Val413Gly
|
|
NM_001368954.1:c.1055T>G
|
NP_001355883.1:p.Val352Gly
|
|