ENST00000367698.4:c.851T>C
MANE Select
|
ENSP00000356671.3:p.Met284Thr
|
|
ENST00000367698.3:c.851T>C
|
ENSP00000356671.3:p.Met284Thr
|
|
ENST00000487183.1:n.502T>C
|
|
|
ENST00000617423.4:c.559+2010T>C
|
ENSP00000478688.1:n.559+2010T>C
|
|
NM_000488.3:c.851T>C , LRG_577t1:c.851T>C
|
NP_000479.1:p.Met284Thr
|
|
XM_005245198.2:c.707T>C
|
XP_005245255.1:p.Met236Thr
|
|
NM_001365052.1:c.707T>C
|
NP_001351981.1:p.Met236Thr
|
|
NM_000488.4:c.851T>C
MANE Select
|
NP_000479.1:p.Met284Thr
|
|
NM_001365052.2:c.707T>C
|
NP_001351981.1:p.Met236Thr
|
|
NM_001386302.1:c.974T>C
|
NP_001373231.1:p.Met325Thr
|
|
NM_001386303.1:c.932T>C
|
NP_001373232.1:p.Met311Thr
|
|
NM_001386304.1:c.830T>C
|
NP_001373233.1:p.Met277Thr
|
|
NM_001386305.1:c.794T>C
|
NP_001373234.1:p.Met265Thr
|
|
NM_001386306.1:c.635T>C
|
NP_001373235.1:p.Met212Thr
|
|