ENST00000367698.4:c.1055T>C
MANE Select
|
ENSP00000356671.3:p.Met352Thr
|
|
ENST00000367698.3:c.1055T>C
|
ENSP00000356671.3:p.Met352Thr
|
|
ENST00000617423.4:c.560-2157T>C
|
ENSP00000478688.1:n.560-2157T>C
|
|
NM_000488.3:c.1055T>C , LRG_577t1:c.1055T>C
|
NP_000479.1:p.Met352Thr
|
|
XM_005245198.2:c.911T>C
|
XP_005245255.1:p.Met304Thr
|
|
NM_001365052.1:c.911T>C
|
NP_001351981.1:p.Met304Thr
|
|
NM_000488.4:c.1055T>C
MANE Select
|
NP_000479.1:p.Met352Thr
|
|
NM_001365052.2:c.911T>C
|
NP_001351981.1:p.Met304Thr
|
|
NM_001386302.1:c.1178T>C
|
NP_001373231.1:p.Met393Thr
|
|
NM_001386303.1:c.1136T>C
|
NP_001373232.1:p.Met379Thr
|
|
NM_001386304.1:c.1034T>C
|
NP_001373233.1:p.Met345Thr
|
|
NM_001386305.1:c.998T>C
|
NP_001373234.1:p.Met333Thr
|
|
NM_001386306.1:c.839T>C
|
NP_001373235.1:p.Met280Thr
|
|