ENST00000367519.9:c.682T>C
MANE Select
|
ENSP00000356489.3:p.Tyr228His
|
|
ENST00000435470.2:c.682T>C
|
ENSP00000405913.2:p.Tyr228His
|
|
ENST00000450221.6:c.304T>C
|
ENSP00000414900.2:p.Tyr102His
|
|
ENST00000611340.5:c.268T>C
|
ENSP00000480268.1:p.Tyr90His
|
|
ENST00000638262.1:c.477-7588T>C
|
ENSP00000492876.1:n.477-7588T>C
|
|
ENST00000638554.1:c.621T>C
|
ENSP00000492823.1:n.621T>C
|
|
ENST00000638717.1:c.465T>C
|
|
|
ENST00000638778.1:c.268T>C
|
ENSP00000491353.1:p.Tyr90His
|
|
ENST00000638783.1:c.268T>C
|
ENSP00000491338.1:p.Tyr90His
|
|
ENST00000639049.1:c.909T>C
|
|
|
ENST00000639423.1:c.268T>C
|
ENSP00000492701.1:p.Tyr90His
|
|
ENST00000639465.1:c.268T>C
|
ENSP00000491180.1:p.Tyr90His
|
|
ENST00000639648.1:n.263T>C
|
|
|
ENST00000639799.1:n.1223T>C
|
|
|
ENST00000639849.1:c.*216T>C
|
ENSP00000491224.1:n.*216T>C
|
|
ENST00000639859.1:n.6006T>C
|
|
|
ENST00000640225.1:c.*216T>C
|
ENSP00000492179.1:n.*216T>C
|
|
ENST00000640351.1:c.418T>C
|
|
|
ENST00000640980.1:c.63-7588T>C
|
ENSP00000491191.1:n.63-7588T>C
|
|
ENST00000367519.7:c.682T>C
|
ENSP00000356489.3:p.Tyr228His
|
|
ENST00000435470.1:c.441T>C
|
|
|
ENST00000450221.5:c.381T>C
|
|
|
ENST00000489412.1:n.301T>C
|
|
|
ENST00000496228.1:n.576T>C
|
|
|
ENST00000611340.4:c.268T>C
|
ENSP00000480268.1:p.Tyr90His
|
|
ENST00000618445.4:c.682T>C
|
ENSP00000480339.1:p.Tyr228His
|
|
NM_001018041.1:c.682T>C
|
NP_001018051.1:p.Tyr228His
|
|
NM_005670.3:c.682T>C
|
NP_005661.1:p.Tyr228His
|
|
XM_006715564.2:c.477-7588T>C
|
XP_006715627.1:n.477-7588T>C
|
|
XM_011536113.1:c.682T>C
|
XP_011534415.1:p.Tyr228His
|
|
XM_011536114.1:c.682T>C
|
XP_011534416.1:p.Tyr228His
|
|
XM_011536116.1:c.268T>C
|
XP_011534418.1:p.Tyr90His
|
|
NM_001360057.1:c.477-7588T>C
|
NP_001346986.1:n.477-7588T>C
|
|
NM_001360064.1:c.268T>C
|
NP_001346993.1:p.Tyr90His
|
|
NM_001360071.1:c.268T>C
|
NP_001347000.1:p.Tyr90His
|
|
NR_153397.1:n.865T>C
|
|
|
NR_153398.1:n.290-7588T>C
|
|
|
XM_011536113.2:c.682T>C
|
XP_011534415.1:p.Tyr228His
|
|
XM_017011301.1:c.220T>C
|
XP_016866790.1:p.Tyr74His
|
|
XM_017011302.1:c.220T>C
|
XP_016866791.1:p.Tyr74His
|
|
XM_024446550.1:c.682T>C
|
XP_024302318.1:p.Tyr228His
|
|
XM_024446551.1:c.268T>C
|
XP_024302319.1:p.Tyr90His
|
|
NM_005670.4:c.682T>C
MANE Select
|
NP_005661.1:p.Tyr228His
|
|
NM_001018041.2:c.682T>C
|
NP_001018051.1:p.Tyr228His
|
|
NM_001360057.2:c.477-7588T>C
|
NP_001346986.1:n.477-7588T>C
|
|
NM_001360064.2:c.268T>C
|
NP_001346993.1:p.Tyr90His
|
|
NM_001360071.2:c.268T>C
|
NP_001347000.1:p.Tyr90His
|
|
NM_001368129.2:c.220T>C
|
NP_001355058.1:p.Tyr74His
|
|
NM_001368130.1:c.682T>C
|
NP_001355059.1:p.Tyr228His
|
|
NM_001368131.1:c.268T>C
|
NP_001355060.1:p.Tyr90His
|
|
NM_001368132.1:c.220T>C
|
NP_001355061.1:p.Tyr74His
|
|
NR_153398.2:n.292-7588T>C
|
|
|