ENST00000309755.9:c.1034T>G
MANE Select
|
ENSP00000312397.4:p.Met345Arg
|
|
ENST00000309755.8:c.1034T>G
|
ENSP00000312397.4:p.Met345Arg
|
|
ENST00000502381.1:n.621T>G
|
|
|
ENST00000504208.5:c.*335-10701T>G
|
ENSP00000423585.1:n.*335-10701T>G
|
|
ENST00000505853.1:c.914T>G
|
ENSP00000426173.1:p.Met305Arg
|
|
ENST00000506491.5:c.788T>G
|
ENSP00000424828.1:p.Met263Arg
|
|
ENST00000506873.5:n.659T>G
|
|
|
ENST00000508657.5:c.938T>G
|
ENSP00000422099.1:p.Met313Arg
|
|
NM_001257194.1:c.938T>G
|
NP_001244123.1:p.Met313Arg
|
|
NM_001257195.1:c.788T>G
|
NP_001244124.1:p.Met263Arg
|
|
NM_017415.2:c.1034T>G
|
NP_059111.2:p.Met345Arg
|
|
NM_017415.3:c.1034T>G
MANE Select
|
NP_059111.2:p.Met345Arg
|
|
NM_001257195.2:c.788T>G
|
NP_001244124.1:p.Met263Arg
|
|