ENST00000688602.1:c.1208C>T
|
|
|
ENST00000689936.1:c.1190C>T
|
|
|
ENST00000359596.8:c.12798C>T
MANE Select
|
ENSP00000352608.2:p.Gly4266=
|
|
ENST00000355481.8:c.12783C>T
|
ENSP00000347667.3:p.Gly4261=
|
|
ENST00000359596.7:c.12798C>T
|
ENSP00000352608.2:p.Gly4266=
|
|
ENST00000360985.7:c.12780C>T
|
ENSP00000354254.4:p.Gly4260=
|
|
ENST00000594335.5:c.6167C>T
|
|
|
NM_000540.2:c.12798C>T , LRG_766t1:c.12798C>T
|
NP_000531.2:p.Gly4266=
|
|
NM_001042723.1:c.12783C>T
|
NP_001036188.1:p.Gly4261=
|
|
XM_006723317.1:c.12780C>T
|
XP_006723380.1:p.Gly4260=
|
|
XM_006723319.1:c.12765C>T
|
XP_006723382.1:p.Gly4255=
|
|
XM_011527204.1:c.12795C>T
|
XP_011525506.1:p.Gly4265=
|
|
XM_011527205.1:c.12798C>T
|
XP_011525507.1:p.Gly4266=
|
|
XM_006723317.2:c.12780C>T
|
XP_006723380.1:p.Gly4260=
|
|
XM_006723319.2:c.12765C>T
|
XP_006723382.1:p.Gly4255=
|
|
XM_011527205.2:c.12798C>T
|
XP_011525507.1:p.Gly4266=
|
|
NM_000540.3:c.12798C>T
MANE Select
|
NP_000531.2:p.Gly4266=
|
|
NM_001042723.2:c.12783C>T
|
NP_001036188.1:p.Gly4261=
|
|