ENST00000650516.2:c.1797C>G
|
ENSP00000498052.2:p.Ser599Arg
|
|
ENST00000343257.7:c.1797C>G
MANE Select
|
ENSP00000339867.2:p.Ser599Arg
|
|
ENST00000432192.6:c.1621C>G
|
|
|
ENST00000343257.6:c.1797C>G
|
ENSP00000339867.2:p.Ser599Arg
|
|
NM_000083.2:c.1797C>G
|
NP_000074.2:p.Ser599Arg
|
|
NR_046453.1:n.1737C>G
|
|
|
XM_011515781.1:c.1821C>G
|
XP_011514083.1:p.Ser607Arg
|
|
XM_011515782.1:c.543C>G
|
XP_011514084.1:p.Ser181Arg
|
|
XM_011515782.2:c.543C>G
|
XP_011514084.1:p.Ser181Arg
|
|
XM_017011739.1:c.1371C>G
|
XP_016867228.1:p.Ser457Arg
|
|
XM_017011740.1:c.1347C>G
|
XP_016867229.1:p.Ser449Arg
|
|
NM_000083.3:c.1797C>G
MANE Select
|
NP_000074.3:p.Ser599Arg
|
|
NR_046453.2:n.1752C>G
|
|
|