ENST00000461073.6:c.*2786G>C
|
ENSP00000419905.1:n.*2786G>C
|
|
ENST00000485349.6:n.4214G>C
|
|
|
ENST00000491994.2:c.*280G>C
|
ENSP00000417586.2:n.*280G>C
|
|
ENST00000494058.6:n.4040G>C
|
|
|
ENST00000697831.1:c.3669G>C
|
ENSP00000513453.1:p.Gln1223His
|
|
ENST00000697832.1:n.3891G>C
|
|
|
ENST00000697834.1:n.4456G>C
|
|
|
ENST00000697835.1:c.*3256G>C
|
ENSP00000513455.1:n.*3256G>C
|
|
ENST00000697837.1:c.*854G>C
|
ENSP00000513456.1:n.*854G>C
|
|
ENST00000697838.1:c.3603G>C
|
ENSP00000513457.1:p.Gln1201His
|
|
ENST00000697839.1:n.4550G>C
|
|
|
ENST00000697840.1:c.3774G>C
|
ENSP00000513458.1:p.Gln1258His
|
|
ENST00000697841.1:n.4649G>C
|
|
|
ENST00000697842.1:n.3993G>C
|
|
|
ENST00000375394.7:c.3738G>C
MANE Select
|
ENSP00000364543.2:p.Gln1246His
|
|
ENST00000375394.6:c.3738G>C
|
ENSP00000364543.2:p.Gln1246His
|
|
ENST00000465703.5:n.4468G>C
|
|
|
ENST00000471818.1:n.667G>C
|
|
|
ENST00000474839.5:c.*3110G>C
|
ENSP00000420470.1:n.*3110G>C
|
|
ENST00000483553.5:c.1268G>C
|
|
|
ENST00000491994.1:c.827G>C
|
|
|
NM_006929.4:c.3738G>C
|
NP_008860.4:p.Gln1246His
|
|
XR_926301.3:n.3754G>C
|
|
|
NM_006929.5:c.3738G>C
MANE Select
|
NP_008860.4:p.Gln1246His
|
|