ENST00000593677.2:c.1816C>T
|
|
|
ENST00000688602.1:c.3213C>T
|
|
|
ENST00000689936.1:c.3185C>T
|
|
|
ENST00000692547.1:n.273C>T
|
|
|
ENST00000359596.8:c.14880C>T
MANE Select
|
ENSP00000352608.2:p.Phe4960=
|
|
ENST00000355481.8:c.14865C>T
|
ENSP00000347667.3:p.Phe4955=
|
|
ENST00000359596.7:c.14880C>T
|
ENSP00000352608.2:p.Phe4960=
|
|
ENST00000360985.7:c.14862C>T
|
ENSP00000354254.4:p.Phe4954=
|
|
NM_000540.2:c.14880C>T , LRG_766t1:c.14880C>T
|
NP_000531.2:p.Phe4960=
|
|
NM_001042723.1:c.14865C>T
|
NP_001036188.1:p.Phe4955=
|
|
XM_006723317.1:c.14862C>T
|
XP_006723380.1:p.Phe4954=
|
|
XM_006723319.1:c.14847C>T
|
XP_006723382.1:p.Phe4949=
|
|
XM_011527204.1:c.14877C>T
|
XP_011525506.1:p.Phe4959=
|
|
XM_011527205.1:c.14793C>T
|
XP_011525507.1:p.Phe4931=
|
|
XM_006723317.2:c.14862C>T
|
XP_006723380.1:p.Phe4954=
|
|
XM_006723319.2:c.14847C>T
|
XP_006723382.1:p.Phe4949=
|
|
XM_011527205.2:c.14793C>T
|
XP_011525507.1:p.Phe4931=
|
|
NM_000540.3:c.14880C>T
MANE Select
|
NP_000531.2:p.Phe4960=
|
|
NM_001042723.2:c.14865C>T
|
NP_001036188.1:p.Phe4955=
|
|