ENST00000299314.12:c.1769C>T
MANE Select
|
ENSP00000299314.7:p.Ser590Phe
|
|
ENST00000299314.11:c.1769C>T
|
ENSP00000299314.7:p.Ser590Phe
|
|
NM_024312.4:c.1769C>T
|
NP_077288.2:p.Ser590Phe
|
|
XM_006719593.2:c.1769C>T
|
XP_006719656.1:p.Ser590Phe
|
|
XM_011538731.1:c.1688C>T
|
XP_011537033.1:p.Ser563Phe
|
|
XM_006719593.3:c.1769C>T
|
XP_006719656.1:p.Ser590Phe
|
|
XM_011538731.2:c.1688C>T
|
XP_011537033.1:p.Ser563Phe
|
|
XM_017019961.1:c.1553C>T
|
XP_016875450.1:p.Ser518Phe
|
|
XM_017019962.2:c.542C>T
|
XP_016875451.1:p.Ser181Phe
|
|
NM_024312.5:c.1769C>T
MANE Select
|
NP_077288.2:p.Ser590Phe
|
|