ENST00000642683.1:c.708T>C
|
ENSP00000495376.1:p.Phe236=
|
|
ENST00000643672.1:c.705T>C
|
ENSP00000494532.1:p.Phe235=
|
|
ENST00000645280.1:c.702T>C
|
ENSP00000496690.1:p.Phe234=
|
|
ENST00000648579.1:c.*53T>C
|
ENSP00000497638.1:n.*53T>C
|
|
ENST00000650617.1:c.756T>C
MANE Select
|
ENSP00000497532.1:p.Phe252=
|
|
ENST00000273158.8:c.756T>C
|
ENSP00000273158.3:p.Phe252=
|
|
NM_017875.2:c.756T>C
|
NP_060345.2:p.Phe252=
|
|
XM_006713214.1:c.744T>C
|
XP_006713277.1:p.Phe248=
|
|
XM_011533869.1:c.738T>C
|
XP_011532171.1:p.Phe246=
|
|
XM_011533870.1:c.705T>C
|
XP_011532172.1:p.Phe235=
|
|
XM_011533871.1:c.576T>C
|
XP_011532173.1:p.Phe192=
|
|
NM_001354798.1:c.626-1858T>C
|
NP_001341727.1:n.626-1858T>C
|
|
NM_017875.4:c.756T>C
MANE Select
|
NP_060345.2:p.Phe252=
|
|
XM_006713214.2:c.744T>C
|
XP_006713277.1:p.Phe248=
|
|
XM_011533869.2:c.738T>C
|
XP_011532171.1:p.Phe246=
|
|
XM_024453611.1:c.702T>C
|
XP_024309379.1:p.Phe234=
|
|
NM_001354798.2:c.626-1858T>C
|
NP_001341727.1:n.626-1858T>C
|
|