ENST00000593677.2:c.735A>T
|
|
|
ENST00000688602.1:c.2132A>T
|
|
|
ENST00000689936.1:c.2104A>T
|
|
|
ENST00000359596.8:c.13799A>T
MANE Select
|
ENSP00000352608.2:p.Asp4600Val
|
|
ENST00000355481.8:c.13784A>T
|
ENSP00000347667.3:p.Asp4595Val
|
|
ENST00000359596.7:c.13799A>T
|
ENSP00000352608.2:p.Asp4600Val
|
|
ENST00000360985.7:c.13781A>T
|
ENSP00000354254.4:p.Asp4594Val
|
|
ENST00000593677.1:c.259A>T
|
|
|
NM_000540.2:c.13799A>T , LRG_766t1:c.13799A>T
|
NP_000531.2:p.Asp4600Val
|
|
NM_001042723.1:c.13784A>T
|
NP_001036188.1:p.Asp4595Val
|
|
XM_006723317.1:c.13781A>T
|
XP_006723380.1:p.Asp4594Val
|
|
XM_006723319.1:c.13766A>T
|
XP_006723382.1:p.Asp4589Val
|
|
XM_011527204.1:c.13796A>T
|
XP_011525506.1:p.Asp4599Val
|
|
XM_011527205.1:c.13712A>T
|
XP_011525507.1:p.Asp4571Val
|
|
XM_006723317.2:c.13781A>T
|
XP_006723380.1:p.Asp4594Val
|
|
XM_006723319.2:c.13766A>T
|
XP_006723382.1:p.Asp4589Val
|
|
XM_011527205.2:c.13712A>T
|
XP_011525507.1:p.Asp4571Val
|
|
NM_000540.3:c.13799A>T
MANE Select
|
NP_000531.2:p.Asp4600Val
|
|
NM_001042723.2:c.13784A>T
|
NP_001036188.1:p.Asp4595Val
|
|