ENST00000684241.1:n.1257G>T
|
|
|
ENST00000262186.10:c.424G>T
MANE Select
|
ENSP00000262186.5:p.Ala142Ser
|
|
ENST00000262186.9:c.424G>T
|
ENSP00000262186.5:p.Ala142Ser
|
|
ENST00000430723.4:c.234+13G>T
|
ENSP00000387657.4:n.234+13G>T
|
|
ENST00000532957.5:n.647G>T
|
|
|
NM_000238.3:c.424G>T , LRG_288t1:c.424G>T
|
NP_000229.1:p.Ala142Ser
|
|
NM_172056.2:c.424G>T , LRG_288t2:c.424G>T
|
NP_742053.1:p.Ala142Ser
|
|
XM_011516185.1:c.124G>T
|
XP_011514487.1:p.Ala42Ser
|
|
XM_011516186.1:c.424G>T
|
XP_011514488.1:p.Ala142Ser
|
|
XM_011516185.2:c.124G>T
|
XP_011514487.1:p.Ala42Ser
|
|
XM_011516186.3:c.424G>T
|
XP_011514488.1:p.Ala142Ser
|
|
XM_017012195.1:c.274G>T
|
XP_016867684.1:p.Ala92Ser
|
|
XM_017012196.1:c.247G>T
|
XP_016867685.1:p.Ala83Ser
|
|
NM_000238.4:c.424G>T
MANE Select
|
NP_000229.1:p.Ala142Ser
|
|