|
ENST00000260947.9:c.1600_1634delinsGCG
MANE Select
|
ENSP00000260947.4:p.Thr534AlafsTer6
|
|
|
ENST00000421162.2:c.247_281delinsGCG
|
ENSP00000392245.2:p.Thr83AlafsTer6
|
|
|
ENST00000613192.2:c.159-22016_159-21982delinsGCG
|
ENSP00000483275.2:n.159-22016_159-21982de...
|
|
|
ENST00000613374.5:c.190_224delinsGCG
|
ENSP00000484464.1:p.Thr64AlafsTer6
|
|
|
ENST00000613706.5:c.1192_1226delinsGCG
|
ENSP00000484976.2:p.Thr398AlafsTer6
|
|
|
ENST00000617164.5:c.1543_1577delinsGCG
|
ENSP00000480470.1:p.Thr515AlafsTer6
|
|
|
ENST00000619009.5:c.365-22016_365-21982delinsGCG
|
ENSP00000482293.1:n.365-22016_365-21982de...
|
|
|
ENST00000650978.1:c.2975_3009delinsGCG
|
|
|
|
ENST00000260947.8:c.1600_1634delinsGCG
|
ENSP00000260947.4:p.Thr534AlafsTer6
|
|
|
ENST00000421162.1:c.247_281delinsGCG
|
ENSP00000392245.1:p.Thr83AlafsTer6
|
|
|
ENST00000455743.5:c.*1220_*1254delinsGCG
|
ENSP00000412186.1:n.*1220_*1254delinsGCG
|
|
|
ENST00000613192.1:c.74-22016_74-21982delinsGCG
|
ENSP00000483275.1:n.74-22016_74-21982deli...
|
|
|
ENST00000613374.4:c.190_224delinsGCG
|
ENSP00000484464.1:p.Thr64AlafsTer6
|
|
|
ENST00000613706.4:c.247_281delinsGCG
|
ENSP00000484976.1:p.Thr83AlafsTer6
|
|
|
ENST00000617164.4:c.1543_1577delinsGCG
|
ENSP00000480470.1:p.Thr515AlafsTer6
|
|
|
ENST00000619009.4:c.365-22016_365-21982delinsGCG
|
ENSP00000482293.1:n.365-22016_365-21982de...
|
|
|
ENST00000620057.4:c.*266_*300delinsGCG
|
ENSP00000481988.1:n.*266_*300delinsGCG
|
|
|
NM_000465.3:c.1600_1634delinsGCG
|
NP_000456.2:p.Thr534AlafsTer6
|
|
|
NM_001282543.1:c.1543_1577delinsGCG
|
NP_001269472.1:p.Thr515AlafsTer6
|
|
|
NM_001282545.1:c.247_281delinsGCG
|
NP_001269474.1:p.Thr83AlafsTer6
|
|
|
NM_001282548.1:c.190_224delinsGCG
|
NP_001269477.1:p.Thr64AlafsTer6
|
|
|
NM_001282549.1:c.365-22016_365-21982delinsGCG
|
NP_001269478.1:n.365-22016_365-21982delin...
|
|
|
NR_104212.1:n.1593_1627delinsGCG
|
|
|
|
NR_104215.1:n.1536_1570delinsGCG
|
|
|
|
NR_104216.1:n.792_826delinsGCG
|
|
|
|
XM_011511567.1:c.1546_1580delinsGCG
|
XP_011509869.1:p.Thr516AlafsTer6
|
|
|
XM_011511568.1:c.1600_1634delinsGCG
|
XP_011509870.1:p.Thr534AlafsTer6
|
|
|
XM_017004613.1:c.1699_1733delinsGCG
|
XP_016860102.1:p.Thr567AlafsTer6
|
|
|
XM_017004614.1:c.1699_1733delinsGCG
|
XP_016860103.1:p.Thr567AlafsTer6
|
|
|
XR_002959322.1:n.1790_1824delinsGCG
|
|
|
|
NM_000465.4:c.1600_1634delinsGCG
MANE Select
|
NP_000456.2:p.Thr534AlafsTer6
|
|
|
NM_001282543.2:c.1543_1577delinsGCG
|
NP_001269472.1:p.Thr515AlafsTer6
|
|
|
NM_001282545.2:c.247_281delinsGCG
|
NP_001269474.1:p.Thr83AlafsTer6
|
|
|
NM_001282548.2:c.190_224delinsGCG
|
NP_001269477.1:p.Thr64AlafsTer6
|
|
|
NM_001282549.2:c.365-22016_365-21982delinsGCG
|
NP_001269478.1:n.365-22016_365-21982delin...
|
|
|
NR_104212.2:n.1565_1599delinsGCG
|
|
|
|
NR_104215.2:n.1508_1542delinsGCG
|
|
|
|
NR_104216.2:n.764_798delinsGCG
|
|
|
