ENST00000684241.1:n.3935C>G
|
|
|
ENST00000262186.10:c.3102C>G
MANE Select
|
ENSP00000262186.5:p.Pro1034=
|
|
ENST00000330883.9:c.2082C>G
|
ENSP00000328531.4:p.Pro694=
|
|
ENST00000262186.9:c.3102C>G
|
ENSP00000262186.5:p.Pro1034=
|
|
ENST00000330883.8:c.2082C>G
|
ENSP00000328531.4:p.Pro694=
|
|
NM_000238.3:c.3102C>G , LRG_288t1:c.3102C>G
|
NP_000229.1:p.Pro1034=
|
|
NM_172057.2:c.2082C>G , LRG_288t3:c.2082C>G
|
NP_742054.1:p.Pro694=
|
|
XM_011516185.1:c.2802C>G
|
XP_011514487.1:p.Pro934=
|
|
XM_011516185.2:c.2802C>G
|
XP_011514487.1:p.Pro934=
|
|
XM_017012195.1:c.2952C>G
|
XP_016867684.1:p.Pro984=
|
|
XM_017012196.1:c.2925C>G
|
XP_016867685.1:p.Pro975=
|
|
NM_000238.4:c.3102C>G
MANE Select
|
NP_000229.1:p.Pro1034=
|
|
NM_172057.3:c.2082C>G
|
NP_742054.1:p.Pro694=
|
|