ENST00000576742.6:c.1688T>A
MANE Select
|
ENSP00000461518.2:p.Leu563His
|
|
ENST00000301365.8:c.1688T>A
|
ENSP00000301365.4:p.Leu563His
|
|
ENST00000381913.8:c.950T>A
|
|
|
ENST00000571139.5:c.*1680T>A
|
ENSP00000458187.1:n.*1680T>A
|
|
ENST00000572519.1:c.1688T>A
|
ENSP00000460215.1:p.Leu563His
|
|
ENST00000573539.5:c.*1698T>A
|
ENSP00000458239.1:n.*1698T>A
|
|
ENST00000576742.5:c.1688T>A
|
ENSP00000461518.1:p.Leu563His
|
|
ENST00000577016.5:c.328+2601T>A
|
|
|
ENST00000616411.4:c.1640T>A
|
ENSP00000483947.1:p.Leu547His
|
|
NM_001258205.1:c.1688T>A
|
NP_001245134.1:p.Leu563His
|
|
NM_145068.3:c.1688T>A
|
NP_659505.1:p.Leu563His
|
|
XM_011523693.1:c.1577+2601T>A
|
XP_011521995.1:n.1577+2601T>A
|
|
XM_011523694.1:c.983T>A
|
XP_011521996.1:p.Leu328His
|
|
XM_011523695.1:c.641T>A
|
XP_011521997.1:p.Leu214His
|
|
XR_934004.1:n.1762T>A
|
|
|
NM_001258205.2:c.1688T>A
|
NP_001245134.1:p.Leu563His
|
|
NM_145068.4:c.1688T>A
MANE Select
|
NP_659505.1:p.Leu563His
|
|