ENST00000355832.10:c.3372T=
MANE Select
|
ENSP00000348089.5:p.Ser1124=
|
|
ENST00000679552.1:n.443T=
|
|
|
ENST00000679871.1:n.518T=
|
|
|
ENST00000679974.1:n.421T=
|
|
|
ENST00000681632.1:n.4775T=
|
|
|
ENST00000681659.1:c.3213T=
|
ENSP00000505631.1:p.Ser1071=
|
|
ENST00000355832.9:c.3372T=
|
ENSP00000348089.5:p.Ser1124=
|
|
ENST00000623073.3:c.*1668T=
|
ENSP00000485650.1:n.*1668T=
|
|
ENST00000623115.3:c.1482T=
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ENSP00000485321.1:p.Ser494=
|
|
ENST00000624341.3:c.1204T=
|
|
|
NM_000124.3:c.3372T=
|
NP_000115.1:p.Ser1124=
|
|
XR_945953.1:n.243-977A=
|
|
|
NM_001346440.1:c.3372T=
|
NP_001333369.1:p.Ser1124=
|
|
NM_000124.4:c.3372T=
MANE Select
|
NP_000115.1:p.Ser1124=
|
|
NM_001346440.2:c.3372T=
|
NP_001333369.1:p.Ser1124=
|
|