ENST00000461073.6:c.*2671G>T
|
ENSP00000419905.1:n.*2671G>T
|
|
ENST00000485349.6:n.4099G>T
|
|
|
ENST00000491994.2:c.*165G>T
|
ENSP00000417586.2:n.*165G>T
|
|
ENST00000494058.6:n.3925G>T
|
|
|
ENST00000697831.1:c.3554G>T
|
ENSP00000513453.1:p.Arg1185Leu
|
|
ENST00000697832.1:n.3776G>T
|
|
|
ENST00000697834.1:n.4341G>T
|
|
|
ENST00000697835.1:c.*3141G>T
|
ENSP00000513455.1:n.*3141G>T
|
|
ENST00000697836.1:n.3977G>T
|
|
|
ENST00000697837.1:c.*739G>T
|
ENSP00000513456.1:n.*739G>T
|
|
ENST00000697838.1:c.3488G>T
|
ENSP00000513457.1:p.Arg1163Leu
|
|
ENST00000697839.1:n.4435G>T
|
|
|
ENST00000697840.1:c.3659G>T
|
ENSP00000513458.1:p.Arg1220Leu
|
|
ENST00000697841.1:n.4534G>T
|
|
|
ENST00000697842.1:n.3878G>T
|
|
|
ENST00000375394.7:c.3623G>T
MANE Select
|
ENSP00000364543.2:p.Arg1208Leu
|
|
ENST00000375394.6:c.3623G>T
|
ENSP00000364543.2:p.Arg1208Leu
|
|
ENST00000465703.5:n.4353G>T
|
|
|
ENST00000471818.1:n.552G>T
|
|
|
ENST00000474839.5:c.*2995G>T
|
ENSP00000420470.1:n.*2995G>T
|
|
ENST00000483553.5:c.1153G>T
|
|
|
ENST00000491994.1:c.712G>T
|
|
|
NM_006929.4:c.3623G>T
|
NP_008860.4:p.Arg1208Leu
|
|
XR_926301.3:n.3639G>T
|
|
|
NM_006929.5:c.3623G>T
MANE Select
|
NP_008860.4:p.Arg1208Leu
|
|