ENST00000578493.2:n.783G>C
|
|
|
ENST00000699291.1:c.575G>C
|
ENSP00000514272.1:p.Ter192Ser
|
|
ENST00000699292.1:n.490G>C
|
|
|
ENST00000225275.4:c.1450G>C
MANE Select
|
ENSP00000225275.3:p.Asp484His
|
|
ENST00000225275.3:c.1450G>C
|
ENSP00000225275.3:p.Asp484His
|
|
NM_000250.1:c.1450G>C , LRG_84t1:c.1450G>C
|
NP_000241.1:p.Asp484His
|
|
XM_011524821.1:c.1636G>C
|
XP_011523123.1:p.Asp546His
|
|
XM_011524822.1:c.1165G>C
|
XP_011523124.1:p.Asp389His
|
|
XM_011524823.1:c.1475G>C
|
XP_011523125.1:p.Ter492Ser
|
|
NM_000250.2:c.1450G>C
MANE Select
|
NP_000241.1:p.Asp484His
|
|