ENST00000578493.2:n.751G>C
|
|
|
ENST00000699291.1:c.543G>C
|
ENSP00000514272.1:p.Glu181Asp
|
|
ENST00000699292.1:n.458G>C
|
|
|
ENST00000225275.4:c.1418G>C
MANE Select
|
ENSP00000225275.3:p.Arg473Thr
|
|
ENST00000225275.3:c.1418G>C
|
ENSP00000225275.3:p.Arg473Thr
|
|
NM_000250.1:c.1418G>C , LRG_84t1:c.1418G>C
|
NP_000241.1:p.Arg473Thr
|
|
XM_011524821.1:c.1604G>C
|
XP_011523123.1:p.Arg535Thr
|
|
XM_011524822.1:c.1133G>C
|
XP_011523124.1:p.Arg378Thr
|
|
XM_011524823.1:c.1443G>C
|
XP_011523125.1:p.Glu481Asp
|
|
NM_000250.2:c.1418G>C
MANE Select
|
NP_000241.1:p.Arg473Thr
|
|