ENST00000367698.4:c.848_853delinsTGATGT
MANE Select
|
ENSP00000356671.3:p.Met283=
|
|
ENST00000367698.3:c.848_853delinsTGATGT
|
ENSP00000356671.3:p.Met283=
|
|
ENST00000487183.1:n.499_504delinsTGATGT
|
|
|
ENST00000617423.4:c.559+2007_559+2012delinsTGATGT
|
ENSP00000478688.1:n.559+2007_559+2012delinsTGATGT
|
|
NM_000488.3:c.848_853delinsTGATGT , LRG_577t1:c.848_853delinsTGATGT
|
NP_000479.1:p.Met283=
|
|
XM_005245198.2:c.704_709delinsTGATGT
|
XP_005245255.1:p.Met235=
|
|
NM_001365052.1:c.704_709delinsTGATGT
|
NP_001351981.1:p.Met235=
|
|
NM_000488.4:c.848_853delinsTGATGT
MANE Select
|
NP_000479.1:p.Met283=
|
|
NM_001365052.2:c.704_709delinsTGATGT
|
NP_001351981.1:p.Met235=
|
|
NM_001386302.1:c.971_976delinsTGATGT
|
NP_001373231.1:p.Met324=
|
|
NM_001386303.1:c.929_934delinsTGATGT
|
NP_001373232.1:p.Met310=
|
|
NM_001386304.1:c.827_832delinsTGATGT
|
NP_001373233.1:p.Met276=
|
|
NM_001386305.1:c.791_796delinsTGATGT
|
NP_001373234.1:p.Met264=
|
|
NM_001386306.1:c.632_637delinsTGATGT
|
NP_001373235.1:p.Met211=
|
|