ENST00000553106.6:c.1247C>G
MANE Select
|
ENSP00000448059.1:p.Pro416Arg
|
|
ENST00000307000.7:c.1232C>G
|
ENSP00000303500.2:p.Pro411Arg
|
|
ENST00000551114.2:n.909C>G
|
|
|
ENST00000553106.5:c.1247C>G
|
ENSP00000448059.1:p.Pro416Arg
|
|
ENST00000635477.1:c.351C>G
|
|
|
ENST00000635528.1:n.762C>G
|
|
|
NM_000277.1:c.1247C>G
|
NP_000268.1:p.Pro416Arg
|
|
XM_011538422.1:c.1190C>G
|
XP_011536724.1:p.Pro397Arg
|
|
NM_000277.2:c.1247C>G
|
NP_000268.1:p.Pro416Arg
|
|
NM_001354304.1:c.1247C>G
|
NP_001341233.1:p.Pro416Arg
|
|
NM_000277.3:c.1247C>G
MANE Select
|
NP_000268.1:p.Pro416Arg
|
|
NM_001354304.2:c.1247C>G
|
NP_001341233.1:p.Pro416Arg
|
|