ENST00000389857.11:c.5158G>T
MANE Select
|
ENSP00000374507.6:p.Glu1720Ter
|
|
ENST00000331194.8:c.730G>T
|
ENSP00000330332.8:p.Glu244Ter
|
|
ENST00000334448.5:n.970G>T
|
|
|
ENST00000389857.10:c.5158G>T
|
ENSP00000374507.6:p.Glu1720Ter
|
|
ENST00000556726.5:c.1386G>T
|
|
|
NM_001080414.3:c.5158G>T
|
NP_001073883.2:p.Glu1720Ter
|
|
XM_011536796.1:c.5050G>T
|
XP_011535098.1:p.Glu1684Ter
|
|
XR_429316.2:n.5433G>T
|
|
|
XM_011536796.2:c.5050G>T
|
XP_011535098.1:p.Glu1684Ter
|
|
XM_017021336.1:c.2239G>T
|
XP_016876825.1:p.Glu747Ter
|
|
XR_429316.4:n.5431G>T
|
|
|
NM_001080414.4:c.5158G>T
MANE Select
|
NP_001073883.2:p.Glu1720Ter
|
|