ENST00000345003.9:c.538A>C
MANE Select
|
ENSP00000340736.4:p.Arg180=
|
|
ENST00000296048.10:c.538A>C
|
ENSP00000296048.6:p.Arg180=
|
|
ENST00000345003.8:c.538A>C
|
ENSP00000340736.4:p.Arg180=
|
|
ENST00000461191.1:c.526A>C
|
ENSP00000420247.1:p.Arg176=
|
|
ENST00000469873.1:n.452A>C
|
|
|
ENST00000479119.1:n.154A>C
|
|
|
ENST00000483267.5:c.469+12440A>C
|
ENSP00000419499.1:n.469+12440A>C
|
|
ENST00000484197.5:c.538A>C
|
ENSP00000420683.1:p.Arg180=
|
|
ENST00000497528.5:n.177A>C
|
|
|
ENST00000627418.2:c.469+12440A>C
|
ENSP00000486061.1:n.469+12440A>C
|
|
NM_001184720.1:c.538A>C
|
NP_001171649.1:p.Arg180=
|
|
NM_001184721.1:c.538A>C
|
NP_001171650.1:p.Arg180=
|
|
NM_004130.3:c.538A>C
|
NP_004121.2:p.Arg180=
|
|
XM_017006275.1:c.361A>C
|
XP_016861764.1:p.Arg121=
|
|
XM_017006276.1:c.76A>C
|
XP_016861765.1:p.Arg26=
|
|
NM_004130.4:c.538A>C
MANE Select
|
NP_004121.2:p.Arg180=
|
|
NM_001184720.2:c.538A>C
|
NP_001171649.1:p.Arg180=
|
|
NM_001184721.2:c.538A>C
|
NP_001171650.1:p.Arg180=
|
|