ENST00000297784.10:c.1756A>T
MANE Select
|
ENSP00000297784.6:p.Met586Leu
|
|
ENST00000644967.1:c.1318A>T
|
ENSP00000496159.1:p.Met440Leu
|
|
ENST00000645053.1:c.1258-10666A>T
|
ENSP00000493838.1:n.1258-10666A>T
|
|
ENST00000645208.2:c.1756A>T
|
ENSP00000494684.1:p.Met586Leu
|
|
ENST00000645773.1:c.1630A>T
|
ENSP00000493698.1:p.Met544Leu
|
|
ENST00000645787.1:n.1899A>T
|
|
|
ENST00000646619.1:c.1318A>T
|
ENSP00000493726.1:p.Met440Leu
|
|
ENST00000651183.1:c.1318A>T
|
ENSP00000498723.1:p.Met440Leu
|
|
ENST00000297784.9:c.1756A>T
|
ENSP00000297784.5:p.Met586Leu
|
|
ENST00000340019.4:c.1756A>T
|
ENSP00000341433.3:p.Met586Leu
|
|
ENST00000469455.1:n.237A>T
|
|
|
ENST00000486417.5:n.380A>T
|
|
|
NM_138691.2:c.1756A>T
|
NP_619636.2:p.Met586Leu
|
|
XM_011518213.1:c.2344A>T
|
XP_011516515.1:p.Met782Leu
|
|
XM_017014256.1:c.1759A>T
|
XP_016869745.1:p.Met587Leu
|
|
NM_138691.3:c.1756A>T
MANE Select
|
NP_619636.2:p.Met586Leu
|
|