ENST00000461073.6:c.*2767C>G
|
ENSP00000419905.1:n.*2767C>G
|
|
ENST00000485349.6:n.4195C>G
|
|
|
ENST00000491994.2:c.*261C>G
|
ENSP00000417586.2:n.*261C>G
|
|
ENST00000494058.6:n.4021C>G
|
|
|
ENST00000697831.1:c.3650C>G
|
ENSP00000513453.1:p.Ala1217Gly
|
|
ENST00000697832.1:n.3872C>G
|
|
|
ENST00000697834.1:n.4437C>G
|
|
|
ENST00000697835.1:c.*3237C>G
|
ENSP00000513455.1:n.*3237C>G
|
|
ENST00000697836.1:n.4073C>G
|
|
|
ENST00000697837.1:c.*835C>G
|
ENSP00000513456.1:n.*835C>G
|
|
ENST00000697838.1:c.3584C>G
|
ENSP00000513457.1:p.Ala1195Gly
|
|
ENST00000697839.1:n.4531C>G
|
|
|
ENST00000697840.1:c.3755C>G
|
ENSP00000513458.1:p.Ala1252Gly
|
|
ENST00000697841.1:n.4630C>G
|
|
|
ENST00000697842.1:n.3974C>G
|
|
|
ENST00000375394.7:c.3719C>G
MANE Select
|
ENSP00000364543.2:p.Ala1240Gly
|
|
ENST00000375394.6:c.3719C>G
|
ENSP00000364543.2:p.Ala1240Gly
|
|
ENST00000465703.5:n.4449C>G
|
|
|
ENST00000471818.1:n.648C>G
|
|
|
ENST00000474839.5:c.*3091C>G
|
ENSP00000420470.1:n.*3091C>G
|
|
ENST00000483553.5:c.1249C>G
|
|
|
ENST00000491994.1:c.808C>G
|
|
|
NM_006929.4:c.3719C>G
|
NP_008860.4:p.Ala1240Gly
|
|
XR_926301.3:n.3735C>G
|
|
|
NM_006929.5:c.3719C>G
MANE Select
|
NP_008860.4:p.Ala1240Gly
|
|