ENST00000527168.6:n.378G>T
|
|
|
ENST00000529110.2:c.363G>T
|
ENSP00000435349.2:p.Glu121Asp
|
|
ENST00000529957.6:n.337G>T
|
|
|
ENST00000683366.1:c.*11G>T
|
ENSP00000507283.1:n.*11G>T
|
|
ENST00000683887.1:c.327G>T
|
ENSP00000506886.1:p.Glu109Asp
|
|
ENST00000684100.1:n.273G>T
|
|
|
ENST00000684126.1:n.337G>T
|
|
|
ENST00000684688.1:n.904G>T
|
|
|
ENST00000204679.9:c.279G>T
MANE Select
|
ENSP00000204679.4:p.Glu93Asp
|
|
ENST00000204679.8:c.279G>T
|
ENSP00000204679.4:p.Glu93Asp
|
|
ENST00000526820.5:c.*181G>T
|
ENSP00000434413.1:n.*181G>T
|
|
ENST00000527076.1:n.1295G>T
|
|
|
ENST00000527168.5:n.315G>T
|
|
|
ENST00000529110.1:c.346G>T
|
|
|
ENST00000529957.5:n.378G>T
|
|
|
NM_032520.4:c.279G>T
|
NP_115909.1:p.Glu93Asp
|
|
XM_017023782.1:c.327G>T
|
XP_016879271.1:p.Glu109Asp
|
|
XM_017023783.1:c.-82G>T
|
XP_016879272.1:n.-82G>T
|
|
NM_032520.5:c.279G>T
MANE Select
|
NP_115909.1:p.Glu93Asp
|
|