ENST00000461073.6:c.*2772A>G
|
ENSP00000419905.1:n.*2772A>G
|
|
ENST00000485349.6:n.4200A>G
|
|
|
ENST00000491994.2:c.*266A>G
|
ENSP00000417586.2:n.*266A>G
|
|
ENST00000494058.6:n.4026A>G
|
|
|
ENST00000697831.1:c.3655A>G
|
ENSP00000513453.1:p.Ser1219Gly
|
|
ENST00000697832.1:n.3877A>G
|
|
|
ENST00000697834.1:n.4442A>G
|
|
|
ENST00000697835.1:c.*3242A>G
|
ENSP00000513455.1:n.*3242A>G
|
|
ENST00000697837.1:c.*840A>G
|
ENSP00000513456.1:n.*840A>G
|
|
ENST00000697838.1:c.3589A>G
|
ENSP00000513457.1:p.Ser1197Gly
|
|
ENST00000697839.1:n.4536A>G
|
|
|
ENST00000697840.1:c.3760A>G
|
ENSP00000513458.1:p.Ser1254Gly
|
|
ENST00000697841.1:n.4635A>G
|
|
|
ENST00000697842.1:n.3979A>G
|
|
|
ENST00000375394.7:c.3724A>G
MANE Select
|
ENSP00000364543.2:p.Ser1242Gly
|
|
ENST00000375394.6:c.3724A>G
|
ENSP00000364543.2:p.Ser1242Gly
|
|
ENST00000465703.5:n.4454A>G
|
|
|
ENST00000471818.1:n.653A>G
|
|
|
ENST00000474839.5:c.*3096A>G
|
ENSP00000420470.1:n.*3096A>G
|
|
ENST00000483553.5:c.1254A>G
|
|
|
ENST00000491994.1:c.813A>G
|
|
|
NM_006929.4:c.3724A>G
|
NP_008860.4:p.Ser1242Gly
|
|
XR_926301.3:n.3740A>G
|
|
|
NM_006929.5:c.3724A>G
MANE Select
|
NP_008860.4:p.Ser1242Gly
|
|