ENST00000317447.9:c.1728A>T
|
ENSP00000320646.4:p.Ser576=
|
|
ENST00000614302.5:c.1728A>T
MANE Select
|
ENSP00000479130.1:p.Ser576=
|
|
ENST00000649953.1:c.1938A>T
|
ENSP00000497456.1:p.Ser646=
|
|
ENST00000317447.8:c.1728A>T
|
ENSP00000320646.4:p.Ser576=
|
|
ENST00000378345.8:c.933A>T
|
ENSP00000367596.4:p.Ser311=
|
|
ENST00000393145.5:n.6638A>T
|
|
|
ENST00000406948.7:c.1728A>T
|
ENSP00000384627.3:p.Ser576=
|
|
ENST00000537116.5:n.854A>T
|
|
|
ENST00000537155.1:n.468A>T
|
|
|
ENST00000542688.5:c.*472A>T
|
ENSP00000446281.1:n.*472A>T
|
|
ENST00000614302.4:c.1728A>T
|
ENSP00000479130.1:p.Ser576=
|
|
NM_001127214.3:c.1728A>T
|
NP_001120686.1:p.Ser576=
|
|
NM_001243279.2:c.1728A>T
|
NP_001230208.1:p.Ser576=
|
|
NM_001284316.1:c.933A>T
|
NP_001271245.1:p.Ser311=
|
|
NM_174917.4:c.1728A>T
|
NP_777577.2:p.Ser576=
|
|
NR_045667.2:n.854A>T
|
|
|
NR_104293.1:n.2162A>T
|
|
|
XR_933239.1:n.2169A>T
|
|
|
XR_933240.1:n.2166A>T
|
|
|
XR_933241.1:n.1923A>T
|
|
|
NR_147928.1:n.2206A>T
|
|
|
NR_147929.1:n.1960A>T
|
|
|
XM_017023020.2:c.-3377A>T
|
XP_016878509.1:n.-3377A>T
|
|
XM_024450187.1:c.933A>T
|
XP_024305955.1:p.Ser311=
|
|
XR_001751864.2:n.1975A>T
|
|
|
XR_933240.3:n.2165A>T
|
|
|
NM_001127214.4:c.1728A>T
|
NP_001120686.1:p.Ser576=
|
|
NM_001243279.3:c.1728A>T
MANE Select
|
NP_001230208.1:p.Ser576=
|
|
NM_001284316.2:c.933A>T
|
NP_001271245.1:p.Ser311=
|
|
NM_174917.5:c.1728A>T
|
NP_777577.2:p.Ser576=
|
|
NR_104293.2:n.2119A>T
|
|
|
NR_147928.2:n.2163A>T
|
|
|
NR_147929.2:n.1917A>T
|
|
|