|
NM_000540.3:c.14860G>T
MANE Select
|
NP_000531.2:p.Asp4954Tyr
|
|
ENST00000359596.8:c.14860G>T
MANE Select
|
ENSP00000352608.2:p.Asp4954Tyr
|
|
NM_000540.2:c.14860G>T , LRG_766t1:c.14860G>T
|
NP_000531.2:p.Asp4954Tyr
|
|
NM_001042723.1:c.14845G>T
|
NP_001036188.1:p.Asp4949Tyr
|
|
NM_001042723.2:c.14845G>T
|
NP_001036188.1:p.Asp4949Tyr
|
|
ENST00000355481.8:c.14845G>T
|
ENSP00000347667.3:p.Asp4949Tyr
|
|
ENST00000359596.7:c.14860G>T
|
ENSP00000352608.2:p.Asp4954Tyr
|
|
ENST00000360985.7:c.14842G>T
|
ENSP00000354254.4:p.Asp4948Tyr
|
|
ENST00000593677.2:c.1796G>T
|
|
|
ENST00000688602.1:c.3193G>T
|
|
|
ENST00000689936.1:c.3165G>T
|
|
|
ENST00000692547.1:n.253G>T
|
|
|
XM_006723317.1:c.14842G>T
|
XP_006723380.1:p.Asp4948Tyr
|
|
XM_006723317.2:c.14842G>T
|
XP_006723380.1:p.Asp4948Tyr
|
|
XM_006723319.1:c.14827G>T
|
XP_006723382.1:p.Asp4943Tyr
|
|
XM_006723319.2:c.14827G>T
|
XP_006723382.1:p.Asp4943Tyr
|
|
XM_011527204.1:c.14857G>T
|
XP_011525506.1:p.Asp4953Tyr
|
|
XM_011527205.1:c.14773G>T
|
XP_011525507.1:p.Asp4925Tyr
|
|
XM_011527205.2:c.14773G>T
|
XP_011525507.1:p.Asp4925Tyr
|
