|
ENST00000593677.2:c.1287T>C
|
|
|
|
ENST00000688602.1:c.2684T>C
|
|
|
|
ENST00000689936.1:c.2656T>C
|
|
|
|
ENST00000359596.8:c.14351T>C
MANE Select
|
ENSP00000352608.2:p.Ile4784Thr
|
|
|
ENST00000355481.8:c.14336T>C
|
ENSP00000347667.3:p.Ile4779Thr
|
|
|
ENST00000359596.7:c.14351T>C
|
ENSP00000352608.2:p.Ile4784Thr
|
|
|
ENST00000360985.7:c.14333T>C
|
ENSP00000354254.4:p.Ile4778Thr
|
|
|
NM_000540.2:c.14351T>C , LRG_766t1:c.14351T>C
|
NP_000531.2:p.Ile4784Thr
|
|
|
NM_001042723.1:c.14336T>C
|
NP_001036188.1:p.Ile4779Thr
|
|
|
XM_006723317.1:c.14333T>C
|
XP_006723380.1:p.Ile4778Thr
|
|
|
XM_006723319.1:c.14318T>C
|
XP_006723382.1:p.Ile4773Thr
|
|
|
XM_011527204.1:c.14348T>C
|
XP_011525506.1:p.Ile4783Thr
|
|
|
XM_011527205.1:c.14264T>C
|
XP_011525507.1:p.Ile4755Thr
|
|
|
XM_006723317.2:c.14333T>C
|
XP_006723380.1:p.Ile4778Thr
|
|
|
XM_006723319.2:c.14318T>C
|
XP_006723382.1:p.Ile4773Thr
|
|
|
XM_011527205.2:c.14264T>C
|
XP_011525507.1:p.Ile4755Thr
|
|
|
NM_000540.3:c.14351T>C
MANE Select
|
NP_000531.2:p.Ile4784Thr
|
|
|
NM_001042723.2:c.14336T>C
|
NP_001036188.1:p.Ile4779Thr
|
|
