ENST00000593677.2:c.914A>T
|
|
|
ENST00000688602.1:c.2311A>T
|
|
|
ENST00000689936.1:c.2283A>T
|
|
|
ENST00000359596.8:c.13978A>T
MANE Select
|
ENSP00000352608.2:p.Ile4660Phe
|
|
ENST00000355481.8:c.13963A>T
|
ENSP00000347667.3:p.Ile4655Phe
|
|
ENST00000359596.7:c.13978A>T
|
ENSP00000352608.2:p.Ile4660Phe
|
|
ENST00000360985.7:c.13960A>T
|
ENSP00000354254.4:p.Ile4654Phe
|
|
NM_000540.2:c.13978A>T , LRG_766t1:c.13978A>T
|
NP_000531.2:p.Ile4660Phe
|
|
NM_001042723.1:c.13963A>T
|
NP_001036188.1:p.Ile4655Phe
|
|
XM_006723317.1:c.13960A>T
|
XP_006723380.1:p.Ile4654Phe
|
|
XM_006723319.1:c.13945A>T
|
XP_006723382.1:p.Ile4649Phe
|
|
XM_011527204.1:c.13975A>T
|
XP_011525506.1:p.Ile4659Phe
|
|
XM_011527205.1:c.13891A>T
|
XP_011525507.1:p.Ile4631Phe
|
|
XM_006723317.2:c.13960A>T
|
XP_006723380.1:p.Ile4654Phe
|
|
XM_006723319.2:c.13945A>T
|
XP_006723382.1:p.Ile4649Phe
|
|
XM_011527205.2:c.13891A>T
|
XP_011525507.1:p.Ile4631Phe
|
|
NM_000540.3:c.13978A>T
MANE Select
|
NP_000531.2:p.Ile4660Phe
|
|
NM_001042723.2:c.13963A>T
|
NP_001036188.1:p.Ile4655Phe
|
|