ENST00000461073.6:c.*2425G>A
|
ENSP00000419905.1:n.*2425G>A
|
|
ENST00000483553.6:c.*438G>A
|
ENSP00000420332.2:n.*438G>A
|
|
ENST00000485349.6:n.3947G>A
|
|
|
ENST00000491994.2:c.3471G>A
|
ENSP00000417586.2:p.Thr1157=
|
|
ENST00000494058.6:n.3773G>A
|
|
|
ENST00000697831.1:c.3402G>A
|
ENSP00000513453.1:p.Thr1134=
|
|
ENST00000697832.1:n.3624G>A
|
|
|
ENST00000697833.1:c.*419G>A
|
ENSP00000513454.1:n.*419G>A
|
|
ENST00000697834.1:n.4095G>A
|
|
|
ENST00000697835.1:c.*2989G>A
|
ENSP00000513455.1:n.*2989G>A
|
|
ENST00000697836.1:n.3802G>A
|
|
|
ENST00000697837.1:c.*587G>A
|
ENSP00000513456.1:n.*587G>A
|
|
ENST00000697838.1:c.3336G>A
|
ENSP00000513457.1:p.Thr1112=
|
|
ENST00000697839.1:n.4189G>A
|
|
|
ENST00000697840.1:c.3507G>A
|
ENSP00000513458.1:p.Thr1169=
|
|
ENST00000697841.1:n.4288G>A
|
|
|
ENST00000697842.1:n.3726G>A
|
|
|
ENST00000375394.7:c.3471G>A
MANE Select
|
ENSP00000364543.2:p.Thr1157=
|
|
ENST00000375394.6:c.3471G>A
|
ENSP00000364543.2:p.Thr1157=
|
|
ENST00000465703.5:n.4107G>A
|
|
|
ENST00000470453.1:n.382+35G>A
|
|
|
ENST00000471818.1:n.400G>A
|
|
|
ENST00000474839.5:c.*2843G>A
|
ENSP00000420470.1:n.*2843G>A
|
|
ENST00000483553.5:c.907G>A
|
|
|
ENST00000485349.5:n.677G>A
|
|
|
ENST00000491994.1:c.466G>A
|
|
|
NM_006929.4:c.3471G>A
|
NP_008860.4:p.Thr1157=
|
|
XR_001743586.2:n.3570G>A
|
|
|
XR_926301.3:n.3487G>A
|
|
|
NM_006929.5:c.3471G>A
MANE Select
|
NP_008860.4:p.Thr1157=
|
|