ENST00000367698.4:c.878G>C
MANE Select
|
ENSP00000356671.3:p.Arg293Pro
|
|
ENST00000367698.3:c.878G>C
|
ENSP00000356671.3:p.Arg293Pro
|
|
ENST00000487183.1:n.529G>C
|
|
|
ENST00000617423.4:c.559+2037G>C
|
ENSP00000478688.1:n.559+2037G>C
|
|
NM_000488.3:c.878G>C , LRG_577t1:c.878G>C
|
NP_000479.1:p.Arg293Pro
|
|
XM_005245198.2:c.734G>C
|
XP_005245255.1:p.Arg245Pro
|
|
NM_001365052.1:c.734G>C
|
NP_001351981.1:p.Arg245Pro
|
|
NM_000488.4:c.878G>C
MANE Select
|
NP_000479.1:p.Arg293Pro
|
|
NM_001365052.2:c.734G>C
|
NP_001351981.1:p.Arg245Pro
|
|
NM_001386302.1:c.1001G>C
|
NP_001373231.1:p.Arg334Pro
|
|
NM_001386303.1:c.959G>C
|
NP_001373232.1:p.Arg320Pro
|
|
NM_001386304.1:c.857G>C
|
NP_001373233.1:p.Arg286Pro
|
|
NM_001386305.1:c.821G>C
|
NP_001373234.1:p.Arg274Pro
|
|
NM_001386306.1:c.662G>C
|
NP_001373235.1:p.Arg221Pro
|
|