ENST00000461073.6:c.*2810A>G
|
ENSP00000419905.1:n.*2810A>G
|
|
ENST00000494058.6:n.4064A>G
|
|
|
ENST00000697831.1:c.*21A>G
|
ENSP00000513453.1:n.*21A>G
|
|
ENST00000697832.1:n.3915A>G
|
|
|
ENST00000697835.1:c.*3280A>G
|
ENSP00000513455.1:n.*3280A>G
|
|
ENST00000697837.1:c.*878A>G
|
ENSP00000513456.1:n.*878A>G
|
|
ENST00000697838.1:c.*21A>G
|
ENSP00000513457.1:n.*21A>G
|
|
ENST00000697840.1:c.*21A>G
|
ENSP00000513458.1:n.*21A>G
|
|
ENST00000697842.1:n.4017A>G
|
|
|
ENST00000375394.7:c.*21A>G
MANE Select
|
ENSP00000364543.2:n.*21A>G
|
|
ENST00000375394.6:c.*21A>G
|
ENSP00000364543.2:n.*21A>G
|
|
ENST00000465703.5:n.4492A>G
|
|
|
ENST00000471818.1:n.691A>G
|
|
|
ENST00000474839.5:c.*3134A>G
|
ENSP00000420470.1:n.*3134A>G
|
|
ENST00000483553.5:c.1292A>G
|
|
|
ENST00000491994.1:c.851A>G
|
|
|
NM_006929.4:c.*21A>G
|
NP_008860.4:n.*21A>G
|
|
XR_926301.3:n.3778A>G
|
|
|
NM_006929.5:c.*21A>G
MANE Select
|
NP_008860.4:n.*21A>G
|
|