ENST00000593677.2:c.1293C>G
|
|
|
ENST00000688602.1:c.2690C>G
|
|
|
ENST00000689936.1:c.2662C>G
|
|
|
ENST00000359596.8:c.14357C>G
MANE Select
|
ENSP00000352608.2:p.Thr4786Arg
|
|
ENST00000355481.8:c.14342C>G
|
ENSP00000347667.3:p.Thr4781Arg
|
|
ENST00000359596.7:c.14357C>G
|
ENSP00000352608.2:p.Thr4786Arg
|
|
ENST00000360985.7:c.14339C>G
|
ENSP00000354254.4:p.Thr4780Arg
|
|
NM_000540.2:c.14357C>G , LRG_766t1:c.14357C>G
|
NP_000531.2:p.Thr4786Arg
|
|
NM_001042723.1:c.14342C>G
|
NP_001036188.1:p.Thr4781Arg
|
|
XM_006723317.1:c.14339C>G
|
XP_006723380.1:p.Thr4780Arg
|
|
XM_006723319.1:c.14324C>G
|
XP_006723382.1:p.Thr4775Arg
|
|
XM_011527204.1:c.14354C>G
|
XP_011525506.1:p.Thr4785Arg
|
|
XM_011527205.1:c.14270C>G
|
XP_011525507.1:p.Thr4757Arg
|
|
XM_006723317.2:c.14339C>G
|
XP_006723380.1:p.Thr4780Arg
|
|
XM_006723319.2:c.14324C>G
|
XP_006723382.1:p.Thr4775Arg
|
|
XM_011527205.2:c.14270C>G
|
XP_011525507.1:p.Thr4757Arg
|
|
NM_000540.3:c.14357C>G
MANE Select
|
NP_000531.2:p.Thr4786Arg
|
|
NM_001042723.2:c.14342C>G
|
NP_001036188.1:p.Thr4781Arg
|
|