ENST00000553106.6:c.706+451A>G
MANE Select
|
ENSP00000448059.1:n.706+451A>G
|
|
ENST00000307000.7:c.691+451A>G
|
ENSP00000303500.2:n.691+451A>G
|
|
ENST00000553106.5:c.706+451A>G
|
ENSP00000448059.1:n.706+451A>G
|
|
NM_000277.1:c.706+451A>G
|
NP_000268.1:n.706+451A>G
|
|
XM_011538422.1:c.706+451A>G
|
XP_011536724.1:n.706+451A>G
|
|
NM_000277.2:c.706+451A>G
|
NP_000268.1:n.706+451A>G
|
|
NM_001354304.1:c.706+451A>G
|
NP_001341233.1:n.706+451A>G
|
|
XM_017019370.2:c.*100A>G
|
XP_016874859.1:n.*100A>G
|
|
NM_000277.3:c.706+451A>G
MANE Select
|
NP_000268.1:n.706+451A>G
|
|
NM_001354304.2:c.706+451A>G
|
NP_001341233.1:n.706+451A>G
|
|