ENST00000684241.1:n.1585C>G
|
|
|
ENST00000262186.10:c.752C>G
MANE Select
|
ENSP00000262186.5:p.Pro251Arg
|
|
ENST00000262186.9:c.752C>G
|
ENSP00000262186.5:p.Pro251Arg
|
|
ENST00000430723.4:c.404C>G
|
ENSP00000387657.4:p.Pro135Arg
|
|
ENST00000532957.5:n.975C>G
|
|
|
NM_000238.3:c.752C>G , LRG_288t1:c.752C>G
|
NP_000229.1:p.Pro251Arg
|
|
NM_172056.2:c.752C>G , LRG_288t2:c.752C>G
|
NP_742053.1:p.Pro251Arg
|
|
XM_011516185.1:c.452C>G
|
XP_011514487.1:p.Pro151Arg
|
|
XM_011516186.1:c.752C>G
|
XP_011514488.1:p.Pro251Arg
|
|
XM_011516185.2:c.452C>G
|
XP_011514487.1:p.Pro151Arg
|
|
XM_011516186.3:c.752C>G
|
XP_011514488.1:p.Pro251Arg
|
|
XM_017012195.1:c.602C>G
|
XP_016867684.1:p.Pro201Arg
|
|
XM_017012196.1:c.575C>G
|
XP_016867685.1:p.Pro192Arg
|
|
NM_000238.4:c.752C>G
MANE Select
|
NP_000229.1:p.Pro251Arg
|
|