ENST00000688602.1:c.357C=
|
|
|
ENST00000689936.1:c.339C=
|
|
|
ENST00000359596.8:c.11947C=
MANE Select
|
ENSP00000352608.2:p.Arg3983=
|
|
ENST00000355481.8:c.11932C=
|
ENSP00000347667.3:p.Arg3978=
|
|
ENST00000359596.7:c.11947C=
|
ENSP00000352608.2:p.Arg3983=
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|
ENST00000360985.7:c.11929C=
|
ENSP00000354254.4:p.Arg3977=
|
|
ENST00000593322.1:c.556C=
|
|
|
ENST00000594335.5:c.5316C=
|
|
|
NM_000540.2:c.11947C= , LRG_766t1:c.11947C=
|
NP_000531.2:p.Arg3983=
|
|
NM_001042723.1:c.11932C=
|
NP_001036188.1:p.Arg3978=
|
|
XM_006723317.1:c.11929C=
|
XP_006723380.1:p.Arg3977=
|
|
XM_006723319.1:c.11914C=
|
XP_006723382.1:p.Arg3972=
|
|
XM_011527204.1:c.11944C=
|
XP_011525506.1:p.Arg3982=
|
|
XM_011527205.1:c.11947C=
|
XP_011525507.1:p.Arg3983=
|
|
XM_006723317.2:c.11929C=
|
XP_006723380.1:p.Arg3977=
|
|
XM_006723319.2:c.11914C=
|
XP_006723382.1:p.Arg3972=
|
|
XM_011527205.2:c.11947C=
|
XP_011525507.1:p.Arg3983=
|
|
NM_000540.3:c.11947C=
MANE Select
|
NP_000531.2:p.Arg3983=
|
|
NM_001042723.2:c.11932C=
|
NP_001036188.1:p.Arg3978=
|
|