ENST00000593677.2:c.1268A>T
|
|
|
ENST00000688602.1:c.2665A>T
|
|
|
ENST00000689936.1:c.2637A>T
|
|
|
ENST00000359596.8:c.14332A>T
MANE Select
|
ENSP00000352608.2:p.Ile4778Phe
|
|
ENST00000355481.8:c.14317A>T
|
ENSP00000347667.3:p.Ile4773Phe
|
|
ENST00000359596.7:c.14332A>T
|
ENSP00000352608.2:p.Ile4778Phe
|
|
ENST00000360985.7:c.14314A>T
|
ENSP00000354254.4:p.Ile4772Phe
|
|
NM_000540.2:c.14332A>T , LRG_766t1:c.14332A>T
|
NP_000531.2:p.Ile4778Phe
|
|
NM_001042723.1:c.14317A>T
|
NP_001036188.1:p.Ile4773Phe
|
|
XM_006723317.1:c.14314A>T
|
XP_006723380.1:p.Ile4772Phe
|
|
XM_006723319.1:c.14299A>T
|
XP_006723382.1:p.Ile4767Phe
|
|
XM_011527204.1:c.14329A>T
|
XP_011525506.1:p.Ile4777Phe
|
|
XM_011527205.1:c.14245A>T
|
XP_011525507.1:p.Ile4749Phe
|
|
XM_006723317.2:c.14314A>T
|
XP_006723380.1:p.Ile4772Phe
|
|
XM_006723319.2:c.14299A>T
|
XP_006723382.1:p.Ile4767Phe
|
|
XM_011527205.2:c.14245A>T
|
XP_011525507.1:p.Ile4749Phe
|
|
NM_000540.3:c.14332A>T
MANE Select
|
NP_000531.2:p.Ile4778Phe
|
|
NM_001042723.2:c.14317A>T
|
NP_001036188.1:p.Ile4773Phe
|
|