ENST00000684241.1:n.1514C>A
|
|
|
ENST00000262186.10:c.681C>A
MANE Select
|
ENSP00000262186.5:p.Pro227=
|
|
ENST00000262186.9:c.681C>A
|
ENSP00000262186.5:p.Pro227=
|
|
ENST00000430723.4:c.333C>A
|
ENSP00000387657.4:p.Pro111=
|
|
ENST00000532957.5:n.904C>A
|
|
|
NM_000238.3:c.681C>A , LRG_288t1:c.681C>A
|
NP_000229.1:p.Pro227=
|
|
NM_172056.2:c.681C>A , LRG_288t2:c.681C>A
|
NP_742053.1:p.Pro227=
|
|
XM_011516185.1:c.381C>A
|
XP_011514487.1:p.Pro127=
|
|
XM_011516186.1:c.681C>A
|
XP_011514488.1:p.Pro227=
|
|
XM_011516185.2:c.381C>A
|
XP_011514487.1:p.Pro127=
|
|
XM_011516186.3:c.681C>A
|
XP_011514488.1:p.Pro227=
|
|
XM_017012195.1:c.531C>A
|
XP_016867684.1:p.Pro177=
|
|
XM_017012196.1:c.504C>A
|
XP_016867685.1:p.Pro168=
|
|
NM_000238.4:c.681C>A
MANE Select
|
NP_000229.1:p.Pro227=
|
|