ENST00000368087.8:c.826A>G
(ARG1)
MANE Select
|
ENSP00000357066.3:p.Met276Val
|
|
ENST00000640973.1:c.605-37A>G
(ARG1)
|
ENSP00000492623.1:n.605-37A>G
|
|
ENST00000672233.1:c.772A>G
(ARG1)
|
ENSP00000499826.1:p.Met258Val
|
|
ENST00000673234.1:c.*713A>G
(ARG1)
|
ENSP00000499885.1:n.*713A>G
|
|
ENST00000673427.1:c.571A>G
(ARG1)
|
ENSP00000500160.1:p.Met191Val
|
|
ENST00000354577.8:c.4095+3944T>C
(MED23)
|
ENSP00000346588.4:n.4095+3944T>C
|
|
ENST00000356962.2:c.850A>G
(ARG1)
|
ENSP00000349446.2:p.Met284Val
|
|
ENST00000368087.7:c.826A>G
(ARG1)
|
ENSP00000357066.3:p.Met276Val
|
|
NM_000045.3:c.826A>G
(ARG1)
|
NP_000036.2:p.Met276Val
|
|
NM_001244438.1:c.850A>G
(ARG1)
|
NP_001231367.1:p.Met284Val
|
|
NM_001270521.1:c.4077+3944T>C
(MED23)
|
NP_001257450.1:n.4077+3944T>C
|
|
NM_015979.3:c.4095+3944T>C
(MED23)
|
NP_057063.2:n.4095+3944T>C
|
|
XM_011535801.1:c.571A>G
(ARG1)
|
XP_011534103.1:p.Met191Val
|
|
XM_011535801.2:c.571A>G
(ARG1)
|
XP_011534103.1:p.Met191Val
|
|
NM_000045.4:c.826A>G
(ARG1)
MANE Select
|
NP_000036.2:p.Met276Val
|
|
NM_001244438.2:c.850A>G
(ARG1)
|
NP_001231367.1:p.Met284Val
|
|
NM_001270521.2:c.4077+3944T>C
(MED23)
|
NP_001257450.1:n.4077+3944T>C
|
|
NM_001369020.1:c.571A>G
(ARG1)
|
NP_001355949.1:p.Met191Val
|
|
NM_015979.4:c.4095+3944T>C
(MED23)
|
NP_057063.2:n.4095+3944T>C
|
|
NR_160934.1:n.810A>G
(ARG1)
|
|
|