ENST00000527168.6:n.434A>G
|
|
|
ENST00000529110.2:c.419A>G
|
ENSP00000435349.2:p.Glu140Gly
|
|
ENST00000529957.6:n.393A>G
|
|
|
ENST00000683366.1:c.*67A>G
|
ENSP00000507283.1:n.*67A>G
|
|
ENST00000683887.1:c.383A>G
|
ENSP00000506886.1:p.Glu128Gly
|
|
ENST00000684100.1:n.329A>G
|
|
|
ENST00000684126.1:n.393A>G
|
|
|
ENST00000684688.1:n.960A>G
|
|
|
ENST00000204679.9:c.335A>G
MANE Select
|
ENSP00000204679.4:p.Glu112Gly
|
|
ENST00000204679.8:c.335A>G
|
ENSP00000204679.4:p.Glu112Gly
|
|
ENST00000526820.5:c.*237A>G
|
ENSP00000434413.1:n.*237A>G
|
|
ENST00000527076.1:n.1351A>G
|
|
|
ENST00000527168.5:n.371A>G
|
|
|
ENST00000529110.1:c.402A>G
|
|
|
ENST00000529957.5:n.434A>G
|
|
|
NM_032520.4:c.335A>G
|
NP_115909.1:p.Glu112Gly
|
|
XM_017023782.1:c.383A>G
|
XP_016879271.1:p.Glu128Gly
|
|
XM_017023783.1:c.-26A>G
|
XP_016879272.1:n.-26A>G
|
|
NM_032520.5:c.335A>G
MANE Select
|
NP_115909.1:p.Glu112Gly
|
|