ENST00000496887.7:c.1001T>A
|
ENSP00000434560.2:p.Leu334Gln
|
|
ENST00000646564.2:c.818T>A
|
ENSP00000495806.2:p.Leu273Gln
|
|
ENST00000155840.12:c.1358T>A
MANE Select
|
ENSP00000155840.2:p.Leu453Gln
|
|
ENST00000335475.6:c.977T>A
|
ENSP00000334497.5:p.Leu326Gln
|
|
ENST00000646564.1:c.464T>A
|
ENSP00000495806.1:p.Leu155Gln
|
|
ENST00000155840.9:c.1358T>A
|
ENSP00000155840.2:p.Leu453Gln
|
|
ENST00000335475.5:c.977T>A
|
ENSP00000334497.5:p.Leu326Gln
|
|
NM_000218.2:c.1358T>A , LRG_287t1:c.1358T>A
|
NP_000209.2:p.Leu453Gln
|
|
NM_181798.1:c.977T>A , LRG_287t2:c.977T>A
|
NP_861463.1:p.Leu326Gln
|
|
NM_000218.3:c.1358T>A
MANE Select
|
NP_000209.2:p.Leu453Gln
|
|