|
ENST00000593677.2:c.1221C=
|
|
|
|
ENST00000688602.1:c.2618C=
|
|
|
|
ENST00000689936.1:c.2590C=
|
|
|
|
ENST00000359596.8:c.14285C=
MANE Select
|
ENSP00000352608.2:p.Pro4762=
|
|
|
ENST00000355481.8:c.14270C=
|
ENSP00000347667.3:p.Pro4757=
|
|
|
ENST00000359596.7:c.14285C=
|
ENSP00000352608.2:p.Pro4762=
|
|
|
ENST00000360985.7:c.14267C=
|
ENSP00000354254.4:p.Pro4756=
|
|
|
NM_000540.2:c.14285C= , LRG_766t1:c.14285C=
|
NP_000531.2:p.Pro4762=
|
|
|
NM_001042723.1:c.14270C=
|
NP_001036188.1:p.Pro4757=
|
|
|
XM_006723317.1:c.14267C=
|
XP_006723380.1:p.Pro4756=
|
|
|
XM_006723319.1:c.14252C=
|
XP_006723382.1:p.Pro4751=
|
|
|
XM_011527204.1:c.14282C=
|
XP_011525506.1:p.Pro4761=
|
|
|
XM_011527205.1:c.14198C=
|
XP_011525507.1:p.Pro4733=
|
|
|
XM_006723317.2:c.14267C=
|
XP_006723380.1:p.Pro4756=
|
|
|
XM_006723319.2:c.14252C=
|
XP_006723382.1:p.Pro4751=
|
|
|
XM_011527205.2:c.14198C=
|
XP_011525507.1:p.Pro4733=
|
|
|
NM_000540.3:c.14285C=
MANE Select
|
NP_000531.2:p.Pro4762=
|
|
|
NM_001042723.2:c.14270C=
|
NP_001036188.1:p.Pro4757=
|
|
