|
ENST00000561514.3:c.3255_3260delinsGTCGTT
|
ENSP00000460666.3:p.Glu1085=
|
|
|
ENST00000565038.2:c.*730_*735delinsGTCGTT
|
ENSP00000459882.2:n.*730_*735delinsGTCGTT...
|
|
|
ENST00000566069.6:c.3202-4296_3202-4291delinsGTCGTT
|
ENSP00000459237.2:n.3202-4296_3202-4291de...
|
|
|
ENST00000697377.2:c.3093_3098delinsGTCGTT
|
ENSP00000513286.2:p.Glu1031=
|
|
|
ENST00000697379.2:c.3255_3260delinsGTCGTT
|
ENSP00000513287.2:p.Glu1085=
|
|
|
ENST00000561514.2:c.2364_2369delinsGTCGTT
|
ENSP00000460666.2:p.Glu788=
|
|
|
ENST00000697374.1:c.2364_2369delinsGTCGTT
|
ENSP00000513284.1:p.Glu788=
|
|
|
ENST00000697375.1:n.4596_4601delinsGTCGTT
|
|
|
|
ENST00000697376.1:c.2317-4296_2317-4291delinsGTCGTT
|
ENSP00000513285.1:n.2317-4296_2317-4291de...
|
|
|
ENST00000697377.1:c.2202_2207delinsGTCGTT
|
ENSP00000513286.1:p.Glu734=
|
|
|
ENST00000697378.1:n.3769_3774delinsGTCGTT
|
|
|
|
ENST00000697379.1:c.2364_2369delinsGTCGTT
|
ENSP00000513287.1:p.Glu788=
|
|
|
ENST00000697380.1:n.2453_2458delinsGTCGTT
|
|
|
|
ENST00000697381.1:n.1944_1949delinsGTCGTT
|
|
|
|
ENST00000697382.1:c.*26_*31delinsGTCGTT
|
ENSP00000513288.1:n.*26_*31delinsGTCGTT
|
|
|
ENST00000697383.1:c.783_788delinsGTCGTT
|
ENSP00000513289.1:p.Glu261=
|
|
|
ENST00000261584.9:c.3249_3254delinsGTCGTT
MANE Select
|
ENSP00000261584.4:p.Glu1083=
|
|
|
ENST00000261584.8:c.3249_3254delinsGTCGTT
|
ENSP00000261584.4:p.Glu1083=
|
|
|
ENST00000566069.5:c.117-4296_117-4291delinsGTCGTT
|
|
|
|
ENST00000568219.5:c.2364_2369delinsGTCGTT
|
ENSP00000454703.2:p.Glu788=
|
|
|
NM_024675.3:c.3249_3254delinsGTCGTT , LRG_308t1:c.3249_3254delinsGTCGTT
|
NP_078951.2:p.Glu1083=
|
|
|
XM_011545946.1:c.3255_3260delinsGTCGTT
|
XP_011544248.1:p.Glu1085=
|
|
|
XM_011545947.1:c.3208-4296_3208-4291delinsGTCGTT
|
XP_011544249.1:n.3208-4296_3208-4291delin...
|
|
|
XM_011545948.1:c.2364_2369delinsGTCGTT
|
XP_011544250.1:p.Glu788=
|
|
|
XR_950851.1:n.3957_3962delinsGTCGTT
|
|
|
|
XM_011545946.2:c.3255_3260delinsGTCGTT
|
XP_011544248.1:p.Glu1085=
|
|
|
XM_011545947.2:c.3208-4296_3208-4291delinsGTCGTT
|
XP_011544249.1:n.3208-4296_3208-4291delin...
|
|
|
XM_011545948.2:c.2364_2369delinsGTCGTT
|
XP_011544250.1:p.Glu788=
|
|
|
XM_017023671.1:c.3120-4296_3120-4291delinsGTCGTT
|
XP_016879160.1:n.3120-4296_3120-4291delin...
|
|
|
XM_017023672.2:c.3114-4296_3114-4291delinsGTCGTT
|
XP_016879161.1:n.3114-4296_3114-4291delin...
|
|
|
XM_017023673.2:c.3202-4296_3202-4291delinsGTCGTT
|
XP_016879162.1:n.3202-4296_3202-4291delin...
|
|
|
NM_024675.4:c.3249_3254delinsGTCGTT
MANE Select
|
NP_078951.2:p.Glu1083=
|
|
