ENST00000461073.6:c.*2448T>A
|
ENSP00000419905.1:n.*2448T>A
|
|
ENST00000483553.6:c.*461T>A
|
ENSP00000420332.2:n.*461T>A
|
|
ENST00000485349.6:n.3970T>A
|
|
|
ENST00000491994.2:c.3494T>A
|
ENSP00000417586.2:p.Leu1165Gln
|
|
ENST00000494058.6:n.3796T>A
|
|
|
ENST00000697831.1:c.3425T>A
|
ENSP00000513453.1:p.Leu1142Gln
|
|
ENST00000697832.1:n.3647T>A
|
|
|
ENST00000697833.1:c.*442T>A
|
ENSP00000513454.1:n.*442T>A
|
|
ENST00000697834.1:n.4118T>A
|
|
|
ENST00000697835.1:c.*3012T>A
|
ENSP00000513455.1:n.*3012T>A
|
|
ENST00000697836.1:n.3825T>A
|
|
|
ENST00000697837.1:c.*610T>A
|
ENSP00000513456.1:n.*610T>A
|
|
ENST00000697838.1:c.3359T>A
|
ENSP00000513457.1:p.Leu1120Gln
|
|
ENST00000697839.1:n.4212T>A
|
|
|
ENST00000697840.1:c.3530T>A
|
ENSP00000513458.1:p.Leu1177Gln
|
|
ENST00000697841.1:n.4311T>A
|
|
|
ENST00000697842.1:n.3749T>A
|
|
|
ENST00000375394.7:c.3494T>A
MANE Select
|
ENSP00000364543.2:p.Leu1165Gln
|
|
ENST00000375394.6:c.3494T>A
|
ENSP00000364543.2:p.Leu1165Gln
|
|
ENST00000465703.5:n.4130T>A
|
|
|
ENST00000470453.1:n.382+58T>A
|
|
|
ENST00000471818.1:n.423T>A
|
|
|
ENST00000474839.5:c.*2866T>A
|
ENSP00000420470.1:n.*2866T>A
|
|
ENST00000483553.5:c.930T>A
|
|
|
ENST00000485349.5:n.700T>A
|
|
|
ENST00000491994.1:c.489T>A
|
|
|
NM_006929.4:c.3494T>A
|
NP_008860.4:p.Leu1165Gln
|
|
XR_001743586.2:n.3593T>A
|
|
|
XR_926301.3:n.3510T>A
|
|
|
NM_006929.5:c.3494T>A
MANE Select
|
NP_008860.4:p.Leu1165Gln
|
|