ENST00000578493.2:n.748T>C
|
|
|
ENST00000699291.1:c.540T>C
|
ENSP00000514272.1:p.His180=
|
|
ENST00000699292.1:n.455T>C
|
|
|
ENST00000225275.4:c.1415T>C
MANE Select
|
ENSP00000225275.3:p.Met472Thr
|
|
ENST00000225275.3:c.1415T>C
|
ENSP00000225275.3:p.Met472Thr
|
|
NM_000250.1:c.1415T>C , LRG_84t1:c.1415T>C
|
NP_000241.1:p.Met472Thr
|
|
XM_011524821.1:c.1601T>C
|
XP_011523123.1:p.Met534Thr
|
|
XM_011524822.1:c.1130T>C
|
XP_011523124.1:p.Met377Thr
|
|
XM_011524823.1:c.1440T>C
|
XP_011523125.1:p.His480=
|
|
NM_000250.2:c.1415T>C
MANE Select
|
NP_000241.1:p.Met472Thr
|
|