ENST00000593677.2:c.1245T>C
|
|
|
ENST00000688602.1:c.2642T>C
|
|
|
ENST00000689936.1:c.2614T>C
|
|
|
ENST00000359596.8:c.14309T>C
MANE Select
|
ENSP00000352608.2:p.Met4770Thr
|
|
ENST00000355481.8:c.14294T>C
|
ENSP00000347667.3:p.Met4765Thr
|
|
ENST00000359596.7:c.14309T>C
|
ENSP00000352608.2:p.Met4770Thr
|
|
ENST00000360985.7:c.14291T>C
|
ENSP00000354254.4:p.Met4764Thr
|
|
NM_000540.2:c.14309T>C , LRG_766t1:c.14309T>C
|
NP_000531.2:p.Met4770Thr
|
|
NM_001042723.1:c.14294T>C
|
NP_001036188.1:p.Met4765Thr
|
|
XM_006723317.1:c.14291T>C
|
XP_006723380.1:p.Met4764Thr
|
|
XM_006723319.1:c.14276T>C
|
XP_006723382.1:p.Met4759Thr
|
|
XM_011527204.1:c.14306T>C
|
XP_011525506.1:p.Met4769Thr
|
|
XM_011527205.1:c.14222T>C
|
XP_011525507.1:p.Met4741Thr
|
|
XM_006723317.2:c.14291T>C
|
XP_006723380.1:p.Met4764Thr
|
|
XM_006723319.2:c.14276T>C
|
XP_006723382.1:p.Met4759Thr
|
|
XM_011527205.2:c.14222T>C
|
XP_011525507.1:p.Met4741Thr
|
|
NM_000540.3:c.14309T>C
MANE Select
|
NP_000531.2:p.Met4770Thr
|
|
NM_001042723.2:c.14294T>C
|
NP_001036188.1:p.Met4765Thr
|
|