|
NM_025243.4:c.962C>T
MANE Select
|
NP_079519.1:p.Ala321Val
|
|
ENST00000644224.2:c.962C>T
MANE Select
|
ENSP00000495385.1:p.Ala321Val
|
|
NM_001371411.1:c.962C>T
|
NP_001358340.1:p.Ala321Val
|
|
NM_001371412.1:c.962C>T
|
NP_001358341.1:p.Ala321Val
|
|
NM_001371413.1:c.950C>T
|
NP_001358342.1:p.Ala317Val
|
|
NM_001371414.1:c.950C>T
|
NP_001358343.1:p.Ala317Val
|
|
NM_025243.3:c.962C>T
|
NP_079519.1:p.Ala321Val
|
|
ENST00000258403.7:c.962C>T
|
ENSP00000258403.3:p.Ala321Val
|
|
ENST00000258403.8:c.962C>T
|
ENSP00000258403.3:p.Ala321Val
|
|
ENST00000409287.5:c.259+703C>T
|
ENSP00000386298.1:n.259+703C>T
|
|
ENST00000425817.5:c.962C>T
|
ENSP00000397393.1:p.Ala321Val
|
|
ENST00000425817.6:c.*987C>T
|
ENSP00000397393.2:n.*987C>T
|
|
ENST00000431622.6:c.*987C>T
|
ENSP00000400627.1:n.*987C>T
|
|
ENST00000642268.1:n.1152C>T
|
|
|
ENST00000645700.1:c.*73C>T
|
ENSP00000495372.1:n.*73C>T
|
|
ENST00000645923.1:c.647C>T
|
ENSP00000495010.1:p.Ala216Val
|
|
ENST00000646591.1:c.998C>T
|
ENSP00000496701.1:p.Ala333Val
|
|
ENST00000647113.1:c.151-2672C>T
|
ENSP00000494966.1:n.151-2672C>T
|
|
ENST00000676066.1:n.692C>T
|
|
|
XM_005246874.2:c.950C>T
|
XP_005246931.1:p.Ala317Val
|
|
XM_005246874.3:c.950C>T
|
XP_005246931.1:p.Ala317Val
|
|
XM_006712779.2:c.977C>T
|
XP_006712842.1:p.Ala326Val
|
|
XM_011511931.1:c.998C>T
|
XP_011510233.1:p.Ala333Val
|
|
XM_011511931.2:c.998C>T
|
XP_011510233.1:p.Ala333Val
|
|
XM_011511932.1:c.962C>T
|
XP_011510234.1:p.Ala321Val
|
|
XM_011511933.1:c.962C>T
|
XP_011510235.1:p.Ala321Val
|
|
XM_017005030.1:c.1202C>T
|
XP_016860519.1:p.Ala401Val
|
|
XM_017005031.1:c.1181C>T
|
XP_016860520.1:p.Ala394Val
|
|
XM_017005032.1:c.1166C>T
|
XP_016860521.1:p.Ala389Val
|
|
XM_017005033.1:c.1166C>T
|
XP_016860522.1:p.Ala389Val
|
|
XM_017005034.2:c.1166C>T
|
XP_016860523.1:p.Ala389Val
|
