ENST00000650516.2:c.1609T>G
|
ENSP00000498052.2:p.Ser537Ala
|
|
ENST00000343257.7:c.1609T>G
MANE Select
|
ENSP00000339867.2:p.Ser537Ala
|
|
ENST00000432192.6:c.1433T>G
|
|
|
ENST00000343257.6:c.1609T>G
|
ENSP00000339867.2:p.Ser537Ala
|
|
NM_000083.2:c.1609T>G
|
NP_000074.2:p.Ser537Ala
|
|
NR_046453.1:n.1549T>G
|
|
|
XM_011515781.1:c.1633T>G
|
XP_011514083.1:p.Ser545Ala
|
|
XM_011515782.1:c.355T>G
|
XP_011514084.1:p.Ser119Ala
|
|
XM_011515782.2:c.355T>G
|
XP_011514084.1:p.Ser119Ala
|
|
XM_017011739.1:c.1183T>G
|
XP_016867228.1:p.Ser395Ala
|
|
XM_017011740.1:c.1159T>G
|
XP_016867229.1:p.Ser387Ala
|
|
NM_000083.3:c.1609T>G
MANE Select
|
NP_000074.3:p.Ser537Ala
|
|
NR_046453.2:n.1564T>G
|
|
|