ENST00000593677.2:c.867T=
|
|
|
ENST00000688602.1:c.2264T=
|
|
|
ENST00000689936.1:c.2236T=
|
|
|
ENST00000359596.8:c.13931T=
MANE Select
|
ENSP00000352608.2:p.Leu4644=
|
|
ENST00000355481.8:c.13916T=
|
ENSP00000347667.3:p.Leu4639=
|
|
ENST00000359596.7:c.13931T=
|
ENSP00000352608.2:p.Leu4644=
|
|
ENST00000360985.7:c.13913T=
|
ENSP00000354254.4:p.Leu4638=
|
|
ENST00000593677.1:c.391T=
|
|
|
NM_000540.2:c.13931T= , LRG_766t1:c.13931T=
|
NP_000531.2:p.Leu4644=
|
|
NM_001042723.1:c.13916T=
|
NP_001036188.1:p.Leu4639=
|
|
XM_006723317.1:c.13913T=
|
XP_006723380.1:p.Leu4638=
|
|
XM_006723319.1:c.13898T=
|
XP_006723382.1:p.Leu4633=
|
|
XM_011527204.1:c.13928T=
|
XP_011525506.1:p.Leu4643=
|
|
XM_011527205.1:c.13844T=
|
XP_011525507.1:p.Leu4615=
|
|
XM_006723317.2:c.13913T=
|
XP_006723380.1:p.Leu4638=
|
|
XM_006723319.2:c.13898T=
|
XP_006723382.1:p.Leu4633=
|
|
XM_011527205.2:c.13844T=
|
XP_011525507.1:p.Leu4615=
|
|
NM_000540.3:c.13931T=
MANE Select
|
NP_000531.2:p.Leu4644=
|
|
NM_001042723.2:c.13916T=
|
NP_001036188.1:p.Leu4639=
|
|