ENST00000599547.6:c.10883G>C
|
ENSP00000471601.2:n.10883G>C
|
|
ENST00000359596.8:c.10944G>C
MANE Select
|
ENSP00000352608.2:p.Arg3648=
|
|
ENST00000355481.8:c.10929G>C
|
ENSP00000347667.3:p.Arg3643=
|
|
ENST00000359596.7:c.10944G>C
|
ENSP00000352608.2:p.Arg3648=
|
|
ENST00000360985.7:c.10926G>C
|
ENSP00000354254.4:p.Arg3642=
|
|
ENST00000594335.5:c.4331G>C
|
|
|
ENST00000599547.5:c.1751G>C
|
|
|
ENST00000601514.5:c.225G>C
|
ENSP00000472497.1:p.Arg75=
|
|
NM_000540.2:c.10944G>C , LRG_766t1:c.10944G>C
|
NP_000531.2:p.Arg3648=
|
|
NM_001042723.1:c.10929G>C
|
NP_001036188.1:p.Arg3643=
|
|
XM_006723317.1:c.10944G>C
|
XP_006723380.1:p.Arg3648=
|
|
XM_006723319.1:c.10929G>C
|
XP_006723382.1:p.Arg3643=
|
|
XM_011527204.1:c.10941G>C
|
XP_011525506.1:p.Arg3647=
|
|
XM_011527205.1:c.10944G>C
|
XP_011525507.1:p.Arg3648=
|
|
XM_006723317.2:c.10944G>C
|
XP_006723380.1:p.Arg3648=
|
|
XM_006723319.2:c.10929G>C
|
XP_006723382.1:p.Arg3643=
|
|
XM_011527205.2:c.10944G>C
|
XP_011525507.1:p.Arg3648=
|
|
NM_000540.3:c.10944G>C
MANE Select
|
NP_000531.2:p.Arg3648=
|
|
NM_001042723.2:c.10929G>C
|
NP_001036188.1:p.Arg3643=
|
|