ENST00000496887.7:c.1193T>C
|
ENSP00000434560.2:p.Ile398Thr
|
|
ENST00000646564.2:c.1010T>C
|
ENSP00000495806.2:p.Ile337Thr
|
|
ENST00000155840.12:c.1550T>C
MANE Select
|
ENSP00000155840.2:p.Ile517Thr
|
|
ENST00000335475.6:c.1169T>C
|
ENSP00000334497.5:p.Ile390Thr
|
|
ENST00000646564.1:c.656T>C
|
ENSP00000495806.1:p.Ile219Thr
|
|
ENST00000155840.9:c.1550T>C
|
ENSP00000155840.2:p.Ile517Thr
|
|
ENST00000335475.5:c.1169T>C
|
ENSP00000334497.5:p.Ile390Thr
|
|
NM_000218.2:c.1550T>C , LRG_287t1:c.1550T>C
|
NP_000209.2:p.Ile517Thr
|
|
NM_181798.1:c.1169T>C , LRG_287t2:c.1169T>C
|
NP_861463.1:p.Ile390Thr
|
|
NM_000218.3:c.1550T>C
MANE Select
|
NP_000209.2:p.Ile517Thr
|
|