ENST00000593677.2:c.1528C>A
|
|
|
ENST00000688602.1:c.2925C>A
|
|
|
ENST00000689936.1:c.2897C>A
|
|
|
ENST00000359596.8:c.14592C>A
MANE Select
|
ENSP00000352608.2:p.Tyr4864Ter
|
|
ENST00000355481.8:c.14577C>A
|
ENSP00000347667.3:p.Tyr4859Ter
|
|
ENST00000359596.7:c.14592C>A
|
ENSP00000352608.2:p.Tyr4864Ter
|
|
ENST00000360985.7:c.14574C>A
|
ENSP00000354254.4:p.Tyr4858Ter
|
|
NM_000540.2:c.14592C>A , LRG_766t1:c.14592C>A
|
NP_000531.2:p.Tyr4864Ter
|
|
NM_001042723.1:c.14577C>A
|
NP_001036188.1:p.Tyr4859Ter
|
|
XM_006723317.1:c.14574C>A
|
XP_006723380.1:p.Tyr4858Ter
|
|
XM_006723319.1:c.14559C>A
|
XP_006723382.1:p.Tyr4853Ter
|
|
XM_011527204.1:c.14589C>A
|
XP_011525506.1:p.Tyr4863Ter
|
|
XM_011527205.1:c.14505C>A
|
XP_011525507.1:p.Tyr4835Ter
|
|
XM_006723317.2:c.14574C>A
|
XP_006723380.1:p.Tyr4858Ter
|
|
XM_006723319.2:c.14559C>A
|
XP_006723382.1:p.Tyr4853Ter
|
|
XM_011527205.2:c.14505C>A
|
XP_011525507.1:p.Tyr4835Ter
|
|
NM_000540.3:c.14592C>A
MANE Select
|
NP_000531.2:p.Tyr4864Ter
|
|
NM_001042723.2:c.14577C>A
|
NP_001036188.1:p.Tyr4859Ter
|
|