ENST00000684241.1:n.1557C>A
|
|
|
ENST00000262186.10:c.724C>A
MANE Select
|
ENSP00000262186.5:p.Arg242Ser
|
|
ENST00000262186.9:c.724C>A
|
ENSP00000262186.5:p.Arg242Ser
|
|
ENST00000430723.4:c.376C>A
|
ENSP00000387657.4:p.Arg126Ser
|
|
ENST00000532957.5:n.947C>A
|
|
|
NM_000238.3:c.724C>A , LRG_288t1:c.724C>A
|
NP_000229.1:p.Arg242Ser
|
|
NM_172056.2:c.724C>A , LRG_288t2:c.724C>A
|
NP_742053.1:p.Arg242Ser
|
|
XM_011516185.1:c.424C>A
|
XP_011514487.1:p.Arg142Ser
|
|
XM_011516186.1:c.724C>A
|
XP_011514488.1:p.Arg242Ser
|
|
XM_011516185.2:c.424C>A
|
XP_011514487.1:p.Arg142Ser
|
|
XM_011516186.3:c.724C>A
|
XP_011514488.1:p.Arg242Ser
|
|
XM_017012195.1:c.574C>A
|
XP_016867684.1:p.Arg192Ser
|
|
XM_017012196.1:c.547C>A
|
XP_016867685.1:p.Arg183Ser
|
|
NM_000238.4:c.724C>A
MANE Select
|
NP_000229.1:p.Arg242Ser
|
|