ENST00000684241.1:n.1470G=
|
|
|
ENST00000262186.10:c.637G=
MANE Select
|
ENSP00000262186.5:p.Asp213=
|
|
ENST00000262186.9:c.637G=
|
ENSP00000262186.5:p.Asp213=
|
|
ENST00000430723.4:c.289G=
|
ENSP00000387657.4:p.Asp97=
|
|
ENST00000532957.5:n.860G=
|
|
|
NM_000238.3:c.637G= , LRG_288t1:c.637G=
|
NP_000229.1:p.Asp213=
|
|
NM_172056.2:c.637G= , LRG_288t2:c.637G=
|
NP_742053.1:p.Asp213=
|
|
XM_011516185.1:c.337G=
|
XP_011514487.1:p.Asp113=
|
|
XM_011516186.1:c.637G=
|
XP_011514488.1:p.Asp213=
|
|
XM_011516185.2:c.337G=
|
XP_011514487.1:p.Asp113=
|
|
XM_011516186.3:c.637G=
|
XP_011514488.1:p.Asp213=
|
|
XM_017012195.1:c.487G=
|
XP_016867684.1:p.Asp163=
|
|
XM_017012196.1:c.460G=
|
XP_016867685.1:p.Asp154=
|
|
NM_000238.4:c.637G=
MANE Select
|
NP_000229.1:p.Asp213=
|
|