ENST00000684241.1:n.1586C>A
|
|
|
ENST00000262186.10:c.753C>A
MANE Select
|
ENSP00000262186.5:p.Pro251=
|
|
ENST00000262186.9:c.753C>A
|
ENSP00000262186.5:p.Pro251=
|
|
ENST00000430723.4:c.405C>A
|
ENSP00000387657.4:p.Pro135=
|
|
ENST00000532957.5:n.976C>A
|
|
|
NM_000238.3:c.753C>A , LRG_288t1:c.753C>A
|
NP_000229.1:p.Pro251=
|
|
NM_172056.2:c.753C>A , LRG_288t2:c.753C>A
|
NP_742053.1:p.Pro251=
|
|
XM_011516185.1:c.453C>A
|
XP_011514487.1:p.Pro151=
|
|
XM_011516186.1:c.753C>A
|
XP_011514488.1:p.Pro251=
|
|
XM_011516185.2:c.453C>A
|
XP_011514487.1:p.Pro151=
|
|
XM_011516186.3:c.753C>A
|
XP_011514488.1:p.Pro251=
|
|
XM_017012195.1:c.603C>A
|
XP_016867684.1:p.Pro201=
|
|
XM_017012196.1:c.576C>A
|
XP_016867685.1:p.Pro192=
|
|
NM_000238.4:c.753C>A
MANE Select
|
NP_000229.1:p.Pro251=
|
|