ENST00000593677.2:c.1838T>C
|
|
|
ENST00000688602.1:c.3235T>C
|
|
|
ENST00000689936.1:c.3207T>C
|
|
|
ENST00000692547.1:n.295T>C
|
|
|
ENST00000359596.8:c.14902T>C
MANE Select
|
ENSP00000352608.2:p.Tyr4968His
|
|
ENST00000355481.8:c.14887T>C
|
ENSP00000347667.3:p.Tyr4963His
|
|
ENST00000359596.7:c.14902T>C
|
ENSP00000352608.2:p.Tyr4968His
|
|
ENST00000360985.7:c.14884T>C
|
ENSP00000354254.4:p.Tyr4962His
|
|
NM_000540.2:c.14902T>C , LRG_766t1:c.14902T>C
|
NP_000531.2:p.Tyr4968His
|
|
NM_001042723.1:c.14887T>C
|
NP_001036188.1:p.Tyr4963His
|
|
XM_006723317.1:c.14884T>C
|
XP_006723380.1:p.Tyr4962His
|
|
XM_006723319.1:c.14869T>C
|
XP_006723382.1:p.Tyr4957His
|
|
XM_011527204.1:c.14899T>C
|
XP_011525506.1:p.Tyr4967His
|
|
XM_011527205.1:c.14815T>C
|
XP_011525507.1:p.Tyr4939His
|
|
XM_006723317.2:c.14884T>C
|
XP_006723380.1:p.Tyr4962His
|
|
XM_006723319.2:c.14869T>C
|
XP_006723382.1:p.Tyr4957His
|
|
XM_011527205.2:c.14815T>C
|
XP_011525507.1:p.Tyr4939His
|
|
NM_000540.3:c.14902T>C
MANE Select
|
NP_000531.2:p.Tyr4968His
|
|
NM_001042723.2:c.14887T>C
|
NP_001036188.1:p.Tyr4963His
|
|