ENST00000496887.7:c.1001T>G
|
ENSP00000434560.2:p.Leu334Arg
|
|
ENST00000646564.2:c.818T>G
|
ENSP00000495806.2:p.Leu273Arg
|
|
ENST00000155840.12:c.1358T>G
MANE Select
|
ENSP00000155840.2:p.Leu453Arg
|
|
ENST00000335475.6:c.977T>G
|
ENSP00000334497.5:p.Leu326Arg
|
|
ENST00000646564.1:c.464T>G
|
ENSP00000495806.1:p.Leu155Arg
|
|
ENST00000155840.9:c.1358T>G
|
ENSP00000155840.2:p.Leu453Arg
|
|
ENST00000335475.5:c.977T>G
|
ENSP00000334497.5:p.Leu326Arg
|
|
NM_000218.2:c.1358T>G , LRG_287t1:c.1358T>G
|
NP_000209.2:p.Leu453Arg
|
|
NM_181798.1:c.977T>G , LRG_287t2:c.977T>G
|
NP_861463.1:p.Leu326Arg
|
|
NM_000218.3:c.1358T>G
MANE Select
|
NP_000209.2:p.Leu453Arg
|
|