ENST00000496887.7:c.1181C>T
|
ENSP00000434560.2:p.Thr394Ile
|
|
ENST00000646564.2:c.998C>T
|
ENSP00000495806.2:p.Thr333Ile
|
|
ENST00000155840.12:c.1538C>T
MANE Select
|
ENSP00000155840.2:p.Thr513Ile
|
|
ENST00000335475.6:c.1157C>T
|
ENSP00000334497.5:p.Thr386Ile
|
|
ENST00000646564.1:c.644C>T
|
ENSP00000495806.1:p.Thr215Ile
|
|
ENST00000155840.9:c.1538C>T
|
ENSP00000155840.2:p.Thr513Ile
|
|
ENST00000335475.5:c.1157C>T
|
ENSP00000334497.5:p.Thr386Ile
|
|
NM_000218.2:c.1538C>T , LRG_287t1:c.1538C>T
|
NP_000209.2:p.Thr513Ile
|
|
NM_181798.1:c.1157C>T , LRG_287t2:c.1157C>T
|
NP_861463.1:p.Thr386Ile
|
|
NM_000218.3:c.1538C>T
MANE Select
|
NP_000209.2:p.Thr513Ile
|
|