ENST00000593677.2:c.1879G>A
|
|
|
ENST00000688602.1:c.3276G>A
|
|
|
ENST00000689936.1:c.3248G>A
|
|
|
ENST00000692547.1:n.336G>A
|
|
|
ENST00000359596.8:c.14943G>A
MANE Select
|
ENSP00000352608.2:p.Leu4981=
|
|
ENST00000355481.8:c.14928G>A
|
ENSP00000347667.3:p.Leu4976=
|
|
ENST00000359596.7:c.14943G>A
|
ENSP00000352608.2:p.Leu4981=
|
|
ENST00000360985.7:c.14925G>A
|
ENSP00000354254.4:p.Leu4975=
|
|
NM_000540.2:c.14943G>A , LRG_766t1:c.14943G>A
|
NP_000531.2:p.Leu4981=
|
|
NM_001042723.1:c.14928G>A
|
NP_001036188.1:p.Leu4976=
|
|
XM_006723317.1:c.14925G>A
|
XP_006723380.1:p.Leu4975=
|
|
XM_006723319.1:c.14910G>A
|
XP_006723382.1:p.Leu4970=
|
|
XM_011527204.1:c.14940G>A
|
XP_011525506.1:p.Leu4980=
|
|
XM_011527205.1:c.14856G>A
|
XP_011525507.1:p.Leu4952=
|
|
XM_006723317.2:c.14925G>A
|
XP_006723380.1:p.Leu4975=
|
|
XM_006723319.2:c.14910G>A
|
XP_006723382.1:p.Leu4970=
|
|
XM_011527205.2:c.14856G>A
|
XP_011525507.1:p.Leu4952=
|
|
NM_000540.3:c.14943G>A
MANE Select
|
NP_000531.2:p.Leu4981=
|
|
NM_001042723.2:c.14928G>A
|
NP_001036188.1:p.Leu4976=
|
|