ENST00000647720.2:c.3417_3420delinsCATG
|
ENSP00000497673.2:p.Ile1139=
|
|
ENST00000647978.2:c.*3131_*3134delinsCATG
|
ENSP00000497658.1:n.*3131_*3134delinsCATG
|
|
ENST00000649781.2:c.3234_3237delinsCATG
|
ENSP00000497203.1:p.Ile1078=
|
|
ENST00000685018.2:c.3417_3420delinsCATG
|
ENSP00000510194.2:p.Ile1139=
|
|
ENST00000687278.2:c.3417_3420delinsCATG
|
ENSP00000509593.2:p.Ile1139=
|
|
ENST00000699585.1:c.3417_3420delinsCATG
|
ENSP00000514456.1:p.Ile1139=
|
|
ENST00000699598.1:c.3417_3420delinsCATG
|
ENSP00000514467.1:p.Ile1139=
|
|
ENST00000699599.1:c.3417_3420delinsCATG
|
ENSP00000514468.1:p.Ile1139=
|
|
ENST00000699600.1:c.3417_3420delinsCATG
|
ENSP00000514469.1:p.Ile1139=
|
|
ENST00000699601.1:c.*1792_*1795delinsCATG
|
ENSP00000514470.1:n.*1792_*1795delinsCATG
|
|
ENST00000699602.1:c.3411_3414delinsCATG
|
ENSP00000514471.1:p.Ile1137=
|
|
ENST00000699604.1:c.*3241_*3244delinsCATG
|
ENSP00000514472.1:n.*3241_*3244delinsCATG
|
|
ENST00000699605.1:c.2991_2994delinsCATG
|
ENSP00000514473.1:p.Ile997=
|
|
ENST00000685018.1:c.165_168delinsCATG
|
ENSP00000510194.1:p.Ile55=
|
|
ENST00000687278.1:c.1008_1011delinsCATG
|
ENSP00000509593.1:p.Ile336=
|
|
ENST00000003084.11:c.3417_3420delinsCATG
MANE Select
|
ENSP00000003084.6:p.Ile1139=
|
|
ENST00000647720.1:c.1067_1070delinsCATG
|
|
|
ENST00000648260.1:c.2199_2202delinsCATG
|
ENSP00000497957.1:p.Ile733=
|
|
ENST00000649406.1:c.3234_3237delinsCATG
|
ENSP00000497965.1:p.Ile1078=
|
|
ENST00000649781.1:c.3234_3237delinsCATG
|
ENSP00000497203.1:p.Ile1078=
|
|
ENST00000003084.10:c.3417_3420delinsCATG
|
ENSP00000003084.6:p.Ile1139=
|
|
ENST00000426809.5:c.3327_3330delinsCATG
|
ENSP00000389119.1:p.Ile1109=
|
|
ENST00000468795.1:c.242_245delinsCATG
|
|
|
NM_000492.3:c.3417_3420delinsCATG , LRG_663t1:c.3417_3420delinsCATG
|
NP_000483.3:p.Ile1139=
|
|
XM_011515751.1:c.3507_3510delinsCATG
|
XP_011514053.1:p.Ile1169=
|
|
XM_011515752.1:c.3507_3510delinsCATG
|
XP_011514054.1:p.Ile1169=
|
|
XM_011515753.1:c.3174_3177delinsCATG
|
XP_011514055.1:p.Ile1058=
|
|
XM_011515754.1:c.3174_3177delinsCATG
|
XP_011514056.1:p.Ile1058=
|
|
NM_000492.4:c.3417_3420delinsCATG
MANE Select
|
NP_000483.3:p.Ile1139=
|
|