|
ENST00000473665.2:n.5187T>G
|
|
|
|
ENST00000482662.2:n.3594T>G
|
|
|
|
ENST00000685865.1:n.1546T>G
|
|
|
|
ENST00000687250.1:n.1246T>G
|
|
|
|
ENST00000687995.1:n.1495T>G
|
|
|
|
ENST00000688205.1:c.*736T>G
|
ENSP00000509673.1:n.*736T>G
|
|
|
ENST00000688788.1:n.1382T>G
|
|
|
|
ENST00000689276.1:c.1074T>G
|
ENSP00000510012.1:p.His358Gln
|
|
|
ENST00000689576.1:c.1143T>G
|
ENSP00000508712.1:p.His381Gln
|
|
|
ENST00000690108.1:c.*799T>G
|
ENSP00000510617.1:n.*799T>G
|
|
|
ENST00000690468.1:c.864T>G
|
ENSP00000509078.1:p.His288Gln
|
|
|
ENST00000690595.1:c.468T>G
|
ENSP00000508979.1:p.His156Gln
|
|
|
ENST00000691348.1:c.972T>G
|
ENSP00000509369.1:p.His324Gln
|
|
|
ENST00000691410.1:c.*720T>G
|
ENSP00000508479.1:n.*720T>G
|
|
|
ENST00000693287.1:c.459T>G
|
ENSP00000510264.1:p.His153Gln
|
|
|
ENST00000693681.1:c.456T>G
|
ENSP00000510789.1:p.His152Gln
|
|
|
ENST00000233838.9:c.1143T>G
MANE Select
|
ENSP00000233838.3:p.His381Gln
|
|
|
ENST00000233838.8:c.1143T>G
|
ENSP00000233838.3:p.His381Gln
|
|
|
ENST00000430215.7:c.972T>G
|
ENSP00000408045.3:p.His324Gln
|
|
|
ENST00000465637.5:n.179-5240T>G
|
|
|
|
ENST00000473665.1:n.636T>G
|
|
|
|
ENST00000482662.1:n.560T>G
|
|
|
|
NM_000821.5:c.1143T>G
|
NP_000812.2:p.His381Gln
|
|
|
NM_000821.6:c.1143T>G
|
NP_000812.2:p.His381Gln
|
|
|
NM_001142269.2:c.972T>G
|
NP_001135741.1:p.His324Gln
|
|
|
NM_001142269.3:c.972T>G
|
NP_001135741.1:p.His324Gln
|
|
|
XM_005264259.3:c.1143T>G
|
XP_005264316.1:p.His381Gln
|
|
|
XM_011532764.1:c.321T>G
|
XP_011531066.1:p.His107Gln
|
|
|
XM_011532765.1:c.321T>G
|
XP_011531067.1:p.His107Gln
|
|
|
XR_939677.1:n.1208T>G
|
|
|
|
XM_005264259.5:c.1143T>G
|
XP_005264316.1:p.His381Gln
|
|
|
XM_011532764.3:c.321T>G
|
XP_011531066.1:p.His107Gln
|
|
|
XM_011532765.3:c.321T>G
|
XP_011531067.1:p.His107Gln
|
|
|
XM_017003803.2:c.972T>G
|
XP_016859292.1:p.His324Gln
|
|
|
XR_001738703.2:n.1208T>G
|
|
|
|
NM_000821.7:c.1143T>G
MANE Select
|
NP_000812.2:p.His381Gln
|
|
|
NM_001142269.4:c.972T>G
|
NP_001135741.1:p.His324Gln
|
|
