|
ENST00000586186.3:c.441+177T>G
|
ENSP00000468273.3:n.441+177T>G
|
|
|
ENST00000587405.6:c.219+177T>G
|
ENSP00000466478.2:n.219+177T>G
|
|
|
ENST00000590016.6:c.636+177T>G
|
ENSP00000466399.1:n.636+177T>G
|
|
|
ENST00000590631.2:n.532+177T>G
|
|
|
|
ENST00000592577.6:c.219+177T>G
|
ENSP00000466839.2:n.219+177T>G
|
|
|
ENST00000345365.11:c.576+177T>G
MANE Select
|
ENSP00000338790.6:n.576+177T>G
|
|
|
ENST00000335858.11:c.240+177T>G
|
ENSP00000338408.6:n.240+177T>G
|
|
|
ENST00000345365.10:c.576+177T>G
|
ENSP00000338790.6:n.576+177T>G
|
|
|
ENST00000394589.8:c.576+177T>G
|
ENSP00000378090.4:n.576+177T>G
|
|
|
ENST00000415064.6:n.767T>G
|
|
|
|
ENST00000460118.6:c.45+177T>G
|
ENSP00000464356.2:n.45+177T>G
|
|
|
ENST00000585947.5:n.649T>G
|
|
|
|
ENST00000586044.5:c.*307+177T>G
|
ENSP00000465584.1:n.*307+177T>G
|
|
|
ENST00000586210.5:c.*170+177T>G
|
ENSP00000465612.1:n.*170+177T>G
|
|
|
ENST00000587405.5:c.219+177T>G
|
ENSP00000466478.1:n.219+177T>G
|
|
|
ENST00000587977.5:c.*316+177T>G
|
ENSP00000466587.1:n.*316+177T>G
|
|
|
ENST00000587982.5:n.546T>G
|
|
|
|
ENST00000588372.5:c.260T>G
|
ENSP00000468764.1:p.Leu87Ter
|
|
|
ENST00000588594.5:c.*172+177T>G
|
ENSP00000465366.1:n.*172+177T>G
|
|
|
ENST00000590016.5:c.636+177T>G
|
ENSP00000466399.1:n.636+177T>G
|
|
|
ENST00000590631.1:c.45+177T>G
|
ENSP00000465033.1:n.45+177T>G
|
|
|
ENST00000591723.5:c.45+177T>G
|
ENSP00000467986.1:n.45+177T>G
|
|
|
ENST00000592181.1:c.219+177T>G
|
ENSP00000464799.1:n.219+177T>G
|
|
|
ENST00000592430.5:n.627T>G
|
|
|
|
ENST00000592577.5:c.582+177T>G
|
ENSP00000466839.1:n.582+177T>G
|
|
|
ENST00000593039.5:c.99+177T>G
|
ENSP00000466834.1:n.99+177T>G
|
|
|
NM_001142571.1:c.636+177T>G
|
NP_001136043.1:n.636+177T>G
|
|
|
NM_002878.3:c.576+177T>G , LRG_516t1:c.576+177T>G
|
NP_002869.3:n.576+177T>G
|
|
|
NM_133629.2:c.240+177T>G
|
NP_598332.1:n.240+177T>G
|
|
|
NR_037711.1:n.713+177T>G
|
|
|
|
NR_037712.1:n.578+177T>G
|
|
|
|
NR_037714.1:n.328+177T>G
|
|
|
|
NM_001142571.2:c.636+177T>G
|
NP_001136043.1:n.636+177T>G
|
|
|
NM_133629.3:c.240+177T>G
|
NP_598332.1:n.240+177T>G
|
|
|
NR_037711.2:n.602+177T>G
|
|
|
|
NR_037712.2:n.467+177T>G
|
|
|
|
NM_002878.4:c.576+177T>G
MANE Select
|
NP_002869.3:n.576+177T>G
|
|
