ENST00000311549.11:c.116T>G
MANE Select
|
ENSP00000346027.4:p.Ile39Ser
|
|
ENST00000272274.8:c.116T>G
|
ENSP00000351021.2:p.Ile39Ser
|
|
ENST00000311549.10:c.116T>G
|
ENSP00000346027.4:p.Ile39Ser
|
|
ENST00000319826.8:c.116T>G
|
ENSP00000370574.1:p.Ile39Ser
|
|
ENST00000326092.8:c.116T>G
|
ENSP00000370569.1:p.Ile39Ser
|
|
ENST00000461690.5:c.116T>G
|
ENSP00000434298.1:p.Ile39Ser
|
|
ENST00000466550.1:n.128T>G
|
|
|
ENST00000473558.5:n.352T>G
|
|
|
ENST00000483765.5:c.67+425T>G
|
ENSP00000473246.1:n.67+425T>G
|
|
ENST00000493317.1:c.116T>G
|
ENSP00000471695.1:p.Ile39Ser
|
|
NM_000982.3:c.116T>G
|
NP_000973.2:p.Ile39Ser
|
|
NM_000982.4:c.116T>G
MANE Select
|
NP_000973.2:p.Ile39Ser
|
|