ENST00000593677.2:c.1957+772C>T
|
|
|
ENST00000688602.1:c.3378C>T
|
|
|
ENST00000689936.1:c.3350C>T
|
|
|
ENST00000692547.1:n.438C>T
|
|
|
ENST00000359596.8:c.15045C>T
MANE Select
|
ENSP00000352608.2:p.Tyr5015=
|
|
ENST00000355481.8:c.15030C>T
|
ENSP00000347667.3:p.Tyr5010=
|
|
ENST00000359596.7:c.15045C>T
|
ENSP00000352608.2:p.Tyr5015=
|
|
ENST00000360985.7:c.15027C>T
|
ENSP00000354254.4:p.Tyr5009=
|
|
NM_000540.2:c.15045C>T , LRG_766t1:c.15045C>T
|
NP_000531.2:p.Tyr5015=
|
|
NM_001042723.1:c.15030C>T
|
NP_001036188.1:p.Tyr5010=
|
|
XM_006723317.1:c.15027C>T
|
XP_006723380.1:p.Tyr5009=
|
|
XM_006723319.1:c.15012C>T
|
XP_006723382.1:p.Tyr5004=
|
|
XM_011527204.1:c.15042C>T
|
XP_011525506.1:p.Tyr5014=
|
|
XM_011527205.1:c.14958C>T
|
XP_011525507.1:p.Tyr4986=
|
|
XM_006723317.2:c.15027C>T
|
XP_006723380.1:p.Tyr5009=
|
|
XM_006723319.2:c.15012C>T
|
XP_006723382.1:p.Tyr5004=
|
|
XM_011527205.2:c.14958C>T
|
XP_011525507.1:p.Tyr4986=
|
|
NM_000540.3:c.15045C>T
MANE Select
|
NP_000531.2:p.Tyr5015=
|
|
NM_001042723.2:c.15030C>T
|
NP_001036188.1:p.Tyr5010=
|
|