ENST00000297784.10:c.1257C>G
MANE Select
|
ENSP00000297784.6:p.Phe419Leu
|
|
ENST00000644967.1:c.819C>G
|
ENSP00000496159.1:p.Phe273Leu
|
|
ENST00000645053.1:c.819C>G
|
ENSP00000493838.1:p.Phe273Leu
|
|
ENST00000645208.2:c.1257C>G
|
ENSP00000494684.1:p.Phe419Leu
|
|
ENST00000645773.1:c.1131C>G
|
ENSP00000493698.1:p.Phe377Leu
|
|
ENST00000645787.1:n.1297C>G
|
|
|
ENST00000646619.1:c.819C>G
|
ENSP00000493726.1:p.Phe273Leu
|
|
ENST00000650689.1:n.1555C>G
|
|
|
ENST00000651183.1:c.819C>G
|
ENSP00000498723.1:p.Phe273Leu
|
|
ENST00000297784.9:c.1257C>G
|
ENSP00000297784.5:p.Phe419Leu
|
|
ENST00000340019.4:c.1257C>G
|
ENSP00000341433.3:p.Phe419Leu
|
|
NM_138691.2:c.1257C>G
|
NP_619636.2:p.Phe419Leu
|
|
XM_011518213.1:c.1845C>G
|
XP_011516515.1:p.Phe615Leu
|
|
XM_017014256.1:c.1260C>G
|
XP_016869745.1:p.Phe420Leu
|
|
NM_138691.3:c.1257C>G
MANE Select
|
NP_619636.2:p.Phe419Leu
|
|