ENST00000593677.2:c.1630dup
|
|
|
ENST00000688602.1:c.3027dup
|
|
|
ENST00000689936.1:c.2999dup
|
|
|
ENST00000692547.1:n.87dup
|
|
|
ENST00000359596.8:c.14694dup
MANE Select
|
ENSP00000352608.2:p.Gly4899TrpfsTer10
|
|
ENST00000355481.8:c.14679dup
|
ENSP00000347667.3:p.Gly4894TrpfsTer10
|
|
ENST00000359596.7:c.14694dup
|
ENSP00000352608.2:p.Gly4899TrpfsTer10
|
|
ENST00000360985.7:c.14676dup
|
ENSP00000354254.4:p.Gly4893TrpfsTer10
|
|
NM_000540.2:c.14694dup , LRG_766t1:c.14694dup
|
NP_000531.2:p.Gly4899TrpfsTer10
|
|
NM_001042723.1:c.14679dup
|
NP_001036188.1:p.Gly4894TrpfsTer10
|
|
XM_006723317.1:c.14676dup
|
XP_006723380.1:p.Gly4893TrpfsTer10
|
|
XM_006723319.1:c.14661dup
|
XP_006723382.1:p.Gly4888TrpfsTer10
|
|
XM_011527204.1:c.14691dup
|
XP_011525506.1:p.Gly4898TrpfsTer10
|
|
XM_011527205.1:c.14607dup
|
XP_011525507.1:p.Gly4870TrpfsTer10
|
|
XM_006723317.2:c.14676dup
|
XP_006723380.1:p.Gly4893TrpfsTer10
|
|
XM_006723319.2:c.14661dup
|
XP_006723382.1:p.Gly4888TrpfsTer10
|
|
XM_011527205.2:c.14607dup
|
XP_011525507.1:p.Gly4870TrpfsTer10
|
|
NM_000540.3:c.14694dup
MANE Select
|
NP_000531.2:p.Gly4899TrpfsTer10
|
|
NM_001042723.2:c.14679dup
|
NP_001036188.1:p.Gly4894TrpfsTer10
|
|