ENST00000684241.1:n.3539A>T
|
|
|
ENST00000262186.10:c.2706A>T
MANE Select
|
ENSP00000262186.5:p.Pro902=
|
|
ENST00000330883.9:c.1686A>T
|
ENSP00000328531.4:p.Pro562=
|
|
ENST00000262186.9:c.2706A>T
|
ENSP00000262186.5:p.Pro902=
|
|
ENST00000330883.8:c.1686A>T
|
ENSP00000328531.4:p.Pro562=
|
|
NM_000238.3:c.2706A>T , LRG_288t1:c.2706A>T
|
NP_000229.1:p.Pro902=
|
|
NM_172057.2:c.1686A>T , LRG_288t3:c.1686A>T
|
NP_742054.1:p.Pro562=
|
|
XM_011516185.1:c.2406A>T
|
XP_011514487.1:p.Pro802=
|
|
XM_011516186.1:c.2693-174A>T
|
XP_011514488.1:n.2693-174A>T
|
|
XM_011516185.2:c.2406A>T
|
XP_011514487.1:p.Pro802=
|
|
XM_011516186.3:c.2693-174A>T
|
XP_011514488.1:n.2693-174A>T
|
|
XM_017012195.1:c.2556A>T
|
XP_016867684.1:p.Pro852=
|
|
XM_017012196.1:c.2529A>T
|
XP_016867685.1:p.Pro843=
|
|
NM_000238.4:c.2706A>T
MANE Select
|
NP_000229.1:p.Pro902=
|
|
NM_172057.3:c.1686A>T
|
NP_742054.1:p.Pro562=
|
|