ENST00000366159.9:n.1840+10G>T
|
|
|
ENST00000437813.8:c.*200+10G>T
|
ENSP00000513672.1:n.*200+10G>T
|
|
ENST00000440083.7:c.958+10G>T
|
ENSP00000413224.3:n.958+10G>T
|
|
ENST00000535038.2:n.921+10G>T
|
|
|
ENST00000535958.2:c.*566+10G>T
|
ENSP00000513673.1:n.*566+10G>T
|
|
ENST00000698337.1:n.729+10G>T
|
|
|
ENST00000698338.1:n.1153+10G>T
|
|
|
ENST00000698339.1:c.*234+10G>T
|
ENSP00000513670.1:n.*234+10G>T
|
|
ENST00000698340.1:c.665+10G>T
|
ENSP00000513671.1:n.665+10G>T
|
|
ENST00000162749.7:c.739+10G>T
MANE Select
|
ENSP00000162749.2:n.739+10G>T
|
|
ENST00000162749.6:c.739+10G>T
|
ENSP00000162749.2:n.739+10G>T
|
|
ENST00000534885.5:c.*216+10G>T
|
ENSP00000441803.1:n.*216+10G>T
|
|
ENST00000535038.1:n.550+10G>T
|
|
|
ENST00000536717.5:n.643+10G>T
|
|
|
ENST00000537842.5:n.343+10G>T
|
|
|
ENST00000539372.5:c.749G>T
|
ENSP00000442059.1:p.Gly250Val
|
|
ENST00000540022.5:c.610+10G>T
|
ENSP00000438343.1:n.610+10G>T
|
|
ENST00000543359.5:n.151+10G>T
|
|
|
ENST00000543995.5:c.*326+10G>T
|
ENSP00000442405.1:n.*326+10G>T
|
|
NM_001065.3:c.739+10G>T , LRG_193t1:c.739+10G>T
|
NP_001056.1:n.739+10G>T
|
|
NM_001346091.1:c.415+10G>T
|
NP_001333020.1:n.415+10G>T
|
|
NM_001346092.1:c.280+10G>T
|
NP_001333021.1:n.280+10G>T
|
|
NR_144351.1:n.968+10G>T
|
|
|
NM_001065.4:c.739+10G>T
MANE Select
|
NP_001056.1:n.739+10G>T
|
|
NM_001346091.2:c.415+10G>T
|
NP_001333020.1:n.415+10G>T
|
|
NM_001346092.2:c.280+10G>T
|
NP_001333021.1:n.280+10G>T
|
|
NR_144351.2:n.927+10G>T
|
|
|