ENST00000688602.1:c.111T>A
|
|
|
ENST00000689936.1:c.93T>A
|
|
|
ENST00000359596.8:c.11701T>A
MANE Select
|
ENSP00000352608.2:p.Tyr3901Asn
|
|
ENST00000355481.8:c.11686T>A
|
ENSP00000347667.3:p.Tyr3896Asn
|
|
ENST00000359596.7:c.11701T>A
|
ENSP00000352608.2:p.Tyr3901Asn
|
|
ENST00000360985.7:c.11683T>A
|
ENSP00000354254.4:p.Tyr3895Asn
|
|
ENST00000593322.1:c.310T>A
|
|
|
ENST00000594335.5:c.5070T>A
|
|
|
NM_000540.2:c.11701T>A , LRG_766t1:c.11701T>A
|
NP_000531.2:p.Tyr3901Asn
|
|
NM_001042723.1:c.11686T>A
|
NP_001036188.1:p.Tyr3896Asn
|
|
XM_006723317.1:c.11683T>A
|
XP_006723380.1:p.Tyr3895Asn
|
|
XM_006723319.1:c.11668T>A
|
XP_006723382.1:p.Tyr3890Asn
|
|
XM_011527204.1:c.11698T>A
|
XP_011525506.1:p.Tyr3900Asn
|
|
XM_011527205.1:c.11701T>A
|
XP_011525507.1:p.Tyr3901Asn
|
|
XM_006723317.2:c.11683T>A
|
XP_006723380.1:p.Tyr3895Asn
|
|
XM_006723319.2:c.11668T>A
|
XP_006723382.1:p.Tyr3890Asn
|
|
XM_011527205.2:c.11701T>A
|
XP_011525507.1:p.Tyr3901Asn
|
|
NM_000540.3:c.11701T>A
MANE Select
|
NP_000531.2:p.Tyr3901Asn
|
|
NM_001042723.2:c.11686T>A
|
NP_001036188.1:p.Tyr3896Asn
|
|