ENST00000461073.6:c.*2617G>T
|
ENSP00000419905.1:n.*2617G>T
|
|
ENST00000485349.6:n.4045G>T
|
|
|
ENST00000491994.2:c.*111G>T
|
ENSP00000417586.2:n.*111G>T
|
|
ENST00000494058.6:n.3871G>T
|
|
|
ENST00000697831.1:c.3500G>T
|
ENSP00000513453.1:p.Gly1167Val
|
|
ENST00000697832.1:n.3722G>T
|
|
|
ENST00000697833.1:c.*517G>T
|
ENSP00000513454.1:n.*517G>T
|
|
ENST00000697834.1:n.4287G>T
|
|
|
ENST00000697835.1:c.*3087G>T
|
ENSP00000513455.1:n.*3087G>T
|
|
ENST00000697836.1:n.3923G>T
|
|
|
ENST00000697837.1:c.*685G>T
|
ENSP00000513456.1:n.*685G>T
|
|
ENST00000697838.1:c.3434G>T
|
ENSP00000513457.1:p.Gly1145Val
|
|
ENST00000697839.1:n.4381G>T
|
|
|
ENST00000697840.1:c.3605G>T
|
ENSP00000513458.1:p.Gly1202Val
|
|
ENST00000697841.1:n.4480G>T
|
|
|
ENST00000697842.1:n.3824G>T
|
|
|
ENST00000375394.7:c.3569G>T
MANE Select
|
ENSP00000364543.2:p.Gly1190Val
|
|
ENST00000375394.6:c.3569G>T
|
ENSP00000364543.2:p.Gly1190Val
|
|
ENST00000465703.5:n.4299G>T
|
|
|
ENST00000470453.1:n.411G>T
|
|
|
ENST00000471818.1:n.498G>T
|
|
|
ENST00000474839.5:c.*2941G>T
|
ENSP00000420470.1:n.*2941G>T
|
|
ENST00000483553.5:c.1099G>T
|
|
|
ENST00000491994.1:c.658G>T
|
|
|
NM_006929.4:c.3569G>T
|
NP_008860.4:p.Gly1190Val
|
|
XR_926301.3:n.3585G>T
|
|
|
NM_006929.5:c.3569G>T
MANE Select
|
NP_008860.4:p.Gly1190Val
|
|