ENST00000461073.6:c.*2474T>C
|
ENSP00000419905.1:n.*2474T>C
|
|
ENST00000483553.6:c.*487T>C
|
ENSP00000420332.2:n.*487T>C
|
|
ENST00000485349.6:n.3996T>C
|
|
|
ENST00000491994.2:c.3520T>C
|
ENSP00000417586.2:p.Tyr1174His
|
|
ENST00000494058.6:n.3822T>C
|
|
|
ENST00000697831.1:c.3451T>C
|
ENSP00000513453.1:p.Tyr1151His
|
|
ENST00000697832.1:n.3673T>C
|
|
|
ENST00000697833.1:c.*468T>C
|
ENSP00000513454.1:n.*468T>C
|
|
ENST00000697834.1:n.4144T>C
|
|
|
ENST00000697835.1:c.*3038T>C
|
ENSP00000513455.1:n.*3038T>C
|
|
ENST00000697836.1:n.3851T>C
|
|
|
ENST00000697837.1:c.*636T>C
|
ENSP00000513456.1:n.*636T>C
|
|
ENST00000697838.1:c.3385T>C
|
ENSP00000513457.1:p.Tyr1129His
|
|
ENST00000697839.1:n.4238T>C
|
|
|
ENST00000697840.1:c.3556T>C
|
ENSP00000513458.1:p.Tyr1186His
|
|
ENST00000697841.1:n.4337T>C
|
|
|
ENST00000697842.1:n.3775T>C
|
|
|
ENST00000375394.7:c.3520T>C
MANE Select
|
ENSP00000364543.2:p.Tyr1174His
|
|
ENST00000375394.6:c.3520T>C
|
ENSP00000364543.2:p.Tyr1174His
|
|
ENST00000465703.5:n.4156T>C
|
|
|
ENST00000470453.1:n.382+84T>C
|
|
|
ENST00000471818.1:n.449T>C
|
|
|
ENST00000474839.5:c.*2892T>C
|
ENSP00000420470.1:n.*2892T>C
|
|
ENST00000483553.5:c.956T>C
|
|
|
ENST00000485349.5:n.726T>C
|
|
|
ENST00000491994.1:c.515T>C
|
|
|
NM_006929.4:c.3520T>C
|
NP_008860.4:p.Tyr1174His
|
|
XR_001743586.2:n.3619T>C
|
|
|
XR_926301.3:n.3536T>C
|
|
|
NM_006929.5:c.3520T>C
MANE Select
|
NP_008860.4:p.Tyr1174His
|
|