ENST00000368087.8:c.921T>G
(ARG1)
MANE Select
|
ENSP00000357066.3:p.Ala307=
|
|
ENST00000640973.1:c.663T>G
(ARG1)
|
ENSP00000492623.1:p.Ala221=
|
|
ENST00000672233.1:c.867T>G
(ARG1)
|
ENSP00000499826.1:p.Ala289=
|
|
ENST00000673234.1:c.*808T>G
(ARG1)
|
ENSP00000499885.1:n.*808T>G
|
|
ENST00000673427.1:c.666T>G
(ARG1)
|
ENSP00000500160.1:p.Ala222=
|
|
ENST00000354577.8:c.4095+3849A>C
(MED23)
|
ENSP00000346588.4:n.4095+3849A>C
|
|
ENST00000356962.2:c.945T>G
(ARG1)
|
ENSP00000349446.2:p.Ala315=
|
|
ENST00000368087.7:c.921T>G
(ARG1)
|
ENSP00000357066.3:p.Ala307=
|
|
NM_000045.3:c.921T>G
(ARG1)
|
NP_000036.2:p.Ala307=
|
|
NM_001244438.1:c.945T>G
(ARG1)
|
NP_001231367.1:p.Ala315=
|
|
NM_001270521.1:c.4077+3849A>C
(MED23)
|
NP_001257450.1:n.4077+3849A>C
|
|
NM_015979.3:c.4095+3849A>C
(MED23)
|
NP_057063.2:n.4095+3849A>C
|
|
XM_011535801.1:c.666T>G
(ARG1)
|
XP_011534103.1:p.Ala222=
|
|
XM_011535801.2:c.666T>G
(ARG1)
|
XP_011534103.1:p.Ala222=
|
|
NM_000045.4:c.921T>G
(ARG1)
MANE Select
|
NP_000036.2:p.Ala307=
|
|
NM_001244438.2:c.945T>G
(ARG1)
|
NP_001231367.1:p.Ala315=
|
|
NM_001270521.2:c.4077+3849A>C
(MED23)
|
NP_001257450.1:n.4077+3849A>C
|
|
NM_001369020.1:c.666T>G
(ARG1)
|
NP_001355949.1:p.Ala222=
|
|
NM_015979.4:c.4095+3849A>C
(MED23)
|
NP_057063.2:n.4095+3849A>C
|
|
NR_160934.1:n.905T>G
(ARG1)
|
|
|