ENST00000368087.8:c.893C>T
(ARG1)
MANE Select
|
ENSP00000357066.3:p.Ala298Val
|
|
ENST00000640973.1:c.635C>T
(ARG1)
|
ENSP00000492623.1:p.Ala212Val
|
|
ENST00000672233.1:c.839C>T
(ARG1)
|
ENSP00000499826.1:p.Ala280Val
|
|
ENST00000673234.1:c.*780C>T
(ARG1)
|
ENSP00000499885.1:n.*780C>T
|
|
ENST00000673427.1:c.638C>T
(ARG1)
|
ENSP00000500160.1:p.Ala213Val
|
|
ENST00000354577.8:c.4095+3877G>A
(MED23)
|
ENSP00000346588.4:n.4095+3877G>A
|
|
ENST00000356962.2:c.917C>T
(ARG1)
|
ENSP00000349446.2:p.Ala306Val
|
|
ENST00000368087.7:c.893C>T
(ARG1)
|
ENSP00000357066.3:p.Ala298Val
|
|
NM_000045.3:c.893C>T
(ARG1)
|
NP_000036.2:p.Ala298Val
|
|
NM_001244438.1:c.917C>T
(ARG1)
|
NP_001231367.1:p.Ala306Val
|
|
NM_001270521.1:c.4077+3877G>A
(MED23)
|
NP_001257450.1:n.4077+3877G>A
|
|
NM_015979.3:c.4095+3877G>A
(MED23)
|
NP_057063.2:n.4095+3877G>A
|
|
XM_011535801.1:c.638C>T
(ARG1)
|
XP_011534103.1:p.Ala213Val
|
|
XM_011535801.2:c.638C>T
(ARG1)
|
XP_011534103.1:p.Ala213Val
|
|
NM_000045.4:c.893C>T
(ARG1)
MANE Select
|
NP_000036.2:p.Ala298Val
|
|
NM_001244438.2:c.917C>T
(ARG1)
|
NP_001231367.1:p.Ala306Val
|
|
NM_001270521.2:c.4077+3877G>A
(MED23)
|
NP_001257450.1:n.4077+3877G>A
|
|
NM_001369020.1:c.638C>T
(ARG1)
|
NP_001355949.1:p.Ala213Val
|
|
NM_015979.4:c.4095+3877G>A
(MED23)
|
NP_057063.2:n.4095+3877G>A
|
|
NR_160934.1:n.877C>T
(ARG1)
|
|
|