ENST00000593677.2:c.1141G>T
|
|
|
ENST00000688602.1:c.2538G>T
|
|
|
ENST00000689936.1:c.2510G>T
|
|
|
ENST00000359596.8:c.14205G>T
MANE Select
|
ENSP00000352608.2:p.Arg4735=
|
|
ENST00000355481.8:c.14190G>T
|
ENSP00000347667.3:p.Arg4730=
|
|
ENST00000359596.7:c.14205G>T
|
ENSP00000352608.2:p.Arg4735=
|
|
ENST00000360985.7:c.14187G>T
|
ENSP00000354254.4:p.Arg4729=
|
|
NM_000540.2:c.14205G>T , LRG_766t1:c.14205G>T
|
NP_000531.2:p.Arg4735=
|
|
NM_001042723.1:c.14190G>T
|
NP_001036188.1:p.Arg4730=
|
|
XM_006723317.1:c.14187G>T
|
XP_006723380.1:p.Arg4729=
|
|
XM_006723319.1:c.14172G>T
|
XP_006723382.1:p.Arg4724=
|
|
XM_011527204.1:c.14202G>T
|
XP_011525506.1:p.Arg4734=
|
|
XM_011527205.1:c.14118G>T
|
XP_011525507.1:p.Arg4706=
|
|
XM_006723317.2:c.14187G>T
|
XP_006723380.1:p.Arg4729=
|
|
XM_006723319.2:c.14172G>T
|
XP_006723382.1:p.Arg4724=
|
|
XM_011527205.2:c.14118G>T
|
XP_011525507.1:p.Arg4706=
|
|
NM_000540.3:c.14205G>T
MANE Select
|
NP_000531.2:p.Arg4735=
|
|
NM_001042723.2:c.14190G>T
|
NP_001036188.1:p.Arg4730=
|
|