ENST00000453170.6:c.2041G>C
|
ENSP00000406377.2:p.Asp681His
|
|
ENST00000524672.3:n.2606G>C
|
|
|
ENST00000700520.1:c.*1878G>C
|
ENSP00000515027.1:n.*1878G>C
|
|
ENST00000700521.1:c.*1921G>C
|
ENSP00000515028.1:n.*1921G>C
|
|
ENST00000700522.1:c.*1921G>C
|
ENSP00000515029.1:n.*1921G>C
|
|
ENST00000700523.1:c.1738G>C
|
ENSP00000515030.1:p.Asp580His
|
|
ENST00000700524.1:c.*1462G>C
|
ENSP00000515031.1:n.*1462G>C
|
|
ENST00000304363.9:c.2254G>C
MANE Select
|
ENSP00000305899.4:p.Asp752His
|
|
ENST00000304363.8:c.2254G>C
|
ENSP00000305899.4:p.Asp752His
|
|
ENST00000441488.6:c.*1462G>C
|
ENSP00000411146.2:n.*1462G>C
|
|
ENST00000615954.4:c.2254G>C
|
ENSP00000484858.1:p.Asp752His
|
|
NM_001300907.1:c.1738G>C
|
NP_001287836.1:p.Asp580His
|
|
NM_001300908.1:c.1534G>C
|
NP_001287837.1:p.Asp512His
|
|
NM_017635.4:c.2254G>C
|
NP_060105.3:p.Asp752His
|
|
XM_005274035.2:c.2254G>C
|
XP_005274092.2:p.Asp752His
|
|
XM_005274036.2:c.2185G>C
|
XP_005274093.2:p.Asp729His
|
|
XM_005274037.1:c.1738G>C
|
XP_005274094.1:p.Asp580His
|
|
XM_006718581.1:c.2185G>C
|
XP_006718644.1:p.Asp729His
|
|
XM_011545091.1:c.2254G>C
|
XP_011543393.1:p.Asp752His
|
|
XM_011545092.1:c.2041G>C
|
XP_011543394.1:p.Asp681His
|
|
XM_011545093.1:c.1012G>C
|
XP_011543395.1:p.Asp338His
|
|
XM_005274035.4:c.2254G>C
|
XP_005274092.2:p.Asp752His
|
|
XM_005274036.4:c.2185G>C
|
XP_005274093.2:p.Asp729His
|
|
XM_006718581.2:c.2185G>C
|
XP_006718644.1:p.Asp729His
|
|
XM_011545092.3:c.2041G>C
|
XP_011543394.1:p.Asp681His
|
|
XM_017017876.2:c.1738G>C
|
XP_016873365.1:p.Asp580His
|
|
XM_017017877.2:c.1738G>C
|
XP_016873366.1:p.Asp580His
|
|
XM_017017878.2:c.1738G>C
|
XP_016873367.1:p.Asp580His
|
|
XM_017017879.2:c.1738G>C
|
XP_016873368.1:p.Asp580His
|
|
XM_024448570.1:c.1012G>C
|
XP_024304338.1:p.Asp338His
|
|
NM_017635.5:c.2254G>C
MANE Select
|
NP_060105.3:p.Asp752His
|
|
NM_001300908.2:c.1534G>C
|
NP_001287837.1:p.Asp512His
|
|
NM_001369426.1:c.2254G>C
|
NP_001356355.1:p.Asp752His
|
|
NM_001369428.1:c.1738G>C
|
NP_001356357.1:p.Asp580His
|
|
NM_001369429.1:c.1738G>C
|
NP_001356358.1:p.Asp580His
|
|
NM_001369430.1:c.1738G>C
|
NP_001356359.1:p.Asp580His
|
|
NM_001369431.1:c.1738G>C
|
NP_001356360.1:p.Asp580His
|
|
NM_001369432.1:c.1738G>C
|
NP_001356361.1:p.Asp580His
|
|
NM_001369433.1:c.1738G>C
|
NP_001356362.1:p.Asp580His
|
|