|
ENST00000367698.4:c.833C>A
MANE Select
|
ENSP00000356671.3:p.Ser278Ter
|
|
|
ENST00000367698.3:c.833C>A
|
ENSP00000356671.3:p.Ser278Ter
|
|
|
ENST00000487183.1:n.484C>A
|
|
|
|
ENST00000617423.4:c.559+1992C>A
|
ENSP00000478688.1:n.559+1992C>A
|
|
|
NM_000488.3:c.833C>A , LRG_577t1:c.833C>A
|
NP_000479.1:p.Ser278Ter
|
|
|
XM_005245198.2:c.689C>A
|
XP_005245255.1:p.Ser230Ter
|
|
|
NM_001365052.1:c.689C>A
|
NP_001351981.1:p.Ser230Ter
|
|
|
NM_000488.4:c.833C>A
MANE Select
|
NP_000479.1:p.Ser278Ter
|
|
|
NM_001365052.2:c.689C>A
|
NP_001351981.1:p.Ser230Ter
|
|
|
NM_001386302.1:c.956C>A
|
NP_001373231.1:p.Ser319Ter
|
|
|
NM_001386303.1:c.914C>A
|
NP_001373232.1:p.Ser305Ter
|
|
|
NM_001386304.1:c.812C>A
|
NP_001373233.1:p.Ser271Ter
|
|
|
NM_001386305.1:c.776C>A
|
NP_001373234.1:p.Ser259Ter
|
|
|
NM_001386306.1:c.617C>A
|
NP_001373235.1:p.Ser206Ter
|
|
