ENST00000261024.7:c.212C>A
MANE Select
|
ENSP00000261024.3:p.Ser71Tyr
|
|
ENST00000261024.6:c.212C>A
|
ENSP00000261024.2:p.Ser71Tyr
|
|
ENST00000418714.1:n.653C>A
|
|
|
ENST00000427241.5:c.212C>A
|
ENSP00000390005.1:p.Ser71Tyr
|
|
ENST00000479598.5:n.493C>A
|
|
|
NM_014585.5:c.212C>A , LRG_837t1:c.212C>A
|
NP_055400.1:p.Ser71Tyr
|
|
XM_005246505.1:c.92C>A
|
XP_005246562.1:p.Ser31Tyr
|
|
XM_005246505.2:c.92C>A
|
XP_005246562.1:p.Ser31Tyr
|
|
XM_017003938.2:c.92C>A
|
XP_016859427.1:p.Ser31Tyr
|
|
NM_014585.6:c.212C>A
MANE Select
|
NP_055400.1:p.Ser71Tyr
|
|