ENST00000369733.8:c.758C>G
|
ENSP00000358748.3:p.Ala253Gly
|
|
ENST00000648076.2:c.758C>G
MANE Select
|
ENSP00000497653.1:p.Ala253Gly
|
|
ENST00000649118.1:n.873C>G
|
|
|
ENST00000650263.1:c.710C>G
|
ENSP00000497850.1:p.Ala237Gly
|
|
ENST00000353479.9:c.758C>G
|
ENSP00000340937.5:p.Ala253Gly
|
|
ENST00000369733.7:c.758C>G
|
ENSP00000358748.3:p.Ala253Gly
|
|
ENST00000393211.3:c.758C>G
|
ENSP00000376905.3:p.Ala253Gly
|
|
ENST00000488320.1:n.103C>G
|
|
|
NM_000494.3:c.758C>G
|
NP_000485.3:p.Ala253Gly
|
|
NM_000494.4:c.758C>G
MANE Select
|
NP_000485.3:p.Ala253Gly
|
|