ENST00000368087.8:c.331C>T
(ARG1)
MANE Select
|
ENSP00000357066.3:p.His111Tyr
|
|
ENST00000640973.1:c.331C>T
(ARG1)
|
ENSP00000492623.1:p.His111Tyr
|
|
ENST00000672233.1:c.277C>T
(ARG1)
|
ENSP00000499826.1:p.His93Tyr
|
|
ENST00000673234.1:c.*218C>T
(ARG1)
|
ENSP00000499885.1:n.*218C>T
|
|
ENST00000673427.1:c.306-1816C>T
(ARG1)
|
ENSP00000500160.1:n.306-1816C>T
|
|
ENST00000275196.5:n.315C>T
(ARG1)
|
|
|
ENST00000354577.8:c.4095+6465G>A
(MED23)
|
ENSP00000346588.4:n.4095+6465G>A
|
|
ENST00000356962.2:c.355C>T
(ARG1)
|
ENSP00000349446.2:p.His119Tyr
|
|
ENST00000368087.7:c.331C>T
(ARG1)
|
ENSP00000357066.3:p.His111Tyr
|
|
NM_000045.3:c.331C>T
(ARG1)
|
NP_000036.2:p.His111Tyr
|
|
NM_001244438.1:c.355C>T
(ARG1)
|
NP_001231367.1:p.His119Tyr
|
|
NM_001270521.1:c.4077+6465G>A
(MED23)
|
NP_001257450.1:n.4077+6465G>A
|
|
NM_015979.3:c.4095+6465G>A
(MED23)
|
NP_057063.2:n.4095+6465G>A
|
|
XM_011535801.1:c.306-1816C>T
(ARG1)
|
XP_011534103.1:n.306-1816C>T
|
|
XM_011535801.2:c.306-1816C>T
(ARG1)
|
XP_011534103.1:n.306-1816C>T
|
|
NM_000045.4:c.331C>T
(ARG1)
MANE Select
|
NP_000036.2:p.His111Tyr
|
|
NM_001244438.2:c.355C>T
(ARG1)
|
NP_001231367.1:p.His119Tyr
|
|
NM_001270521.2:c.4077+6465G>A
(MED23)
|
NP_001257450.1:n.4077+6465G>A
|
|
NM_001369020.1:c.306-1816C>T
(ARG1)
|
NP_001355949.1:n.306-1816C>T
|
|
NM_015979.4:c.4095+6465G>A
(MED23)
|
NP_057063.2:n.4095+6465G>A
|
|
NR_160934.1:n.315C>T
(ARG1)
|
|
|