ENST00000593677.2:c.843G>C
|
|
|
ENST00000688602.1:c.2240G>C
|
|
|
ENST00000689936.1:c.2212G>C
|
|
|
ENST00000359596.8:c.13907G>C
MANE Select
|
ENSP00000352608.2:p.Ser4636Thr
|
|
ENST00000355481.8:c.13892G>C
|
ENSP00000347667.3:p.Ser4631Thr
|
|
ENST00000359596.7:c.13907G>C
|
ENSP00000352608.2:p.Ser4636Thr
|
|
ENST00000360985.7:c.13889G>C
|
ENSP00000354254.4:p.Ser4630Thr
|
|
ENST00000593677.1:c.367G>C
|
|
|
NM_000540.2:c.13907G>C , LRG_766t1:c.13907G>C
|
NP_000531.2:p.Ser4636Thr
|
|
NM_001042723.1:c.13892G>C
|
NP_001036188.1:p.Ser4631Thr
|
|
XM_006723317.1:c.13889G>C
|
XP_006723380.1:p.Ser4630Thr
|
|
XM_006723319.1:c.13874G>C
|
XP_006723382.1:p.Ser4625Thr
|
|
XM_011527204.1:c.13904G>C
|
XP_011525506.1:p.Ser4635Thr
|
|
XM_011527205.1:c.13820G>C
|
XP_011525507.1:p.Ser4607Thr
|
|
XM_006723317.2:c.13889G>C
|
XP_006723380.1:p.Ser4630Thr
|
|
XM_006723319.2:c.13874G>C
|
XP_006723382.1:p.Ser4625Thr
|
|
XM_011527205.2:c.13820G>C
|
XP_011525507.1:p.Ser4607Thr
|
|
NM_000540.3:c.13907G>C
MANE Select
|
NP_000531.2:p.Ser4636Thr
|
|
NM_001042723.2:c.13892G>C
|
NP_001036188.1:p.Ser4631Thr
|
|