ENST00000684241.1:n.1587C>G
|
|
|
ENST00000262186.10:c.754C>G
MANE Select
|
ENSP00000262186.5:p.Arg252Gly
|
|
ENST00000262186.9:c.754C>G
|
ENSP00000262186.5:p.Arg252Gly
|
|
ENST00000430723.4:c.406C>G
|
ENSP00000387657.4:p.Arg136Gly
|
|
ENST00000532957.5:n.977C>G
|
|
|
NM_000238.3:c.754C>G , LRG_288t1:c.754C>G
|
NP_000229.1:p.Arg252Gly
|
|
NM_172056.2:c.754C>G , LRG_288t2:c.754C>G
|
NP_742053.1:p.Arg252Gly
|
|
XM_011516185.1:c.454C>G
|
XP_011514487.1:p.Arg152Gly
|
|
XM_011516186.1:c.754C>G
|
XP_011514488.1:p.Arg252Gly
|
|
XM_011516185.2:c.454C>G
|
XP_011514487.1:p.Arg152Gly
|
|
XM_011516186.3:c.754C>G
|
XP_011514488.1:p.Arg252Gly
|
|
XM_017012195.1:c.604C>G
|
XP_016867684.1:p.Arg202Gly
|
|
XM_017012196.1:c.577C>G
|
XP_016867685.1:p.Arg193Gly
|
|
NM_000238.4:c.754C>G
MANE Select
|
NP_000229.1:p.Arg252Gly
|
|