ENST00000295897.9:c.1459T>A
MANE Select
|
ENSP00000295897.4:p.Leu487Met
|
|
ENST00000295897.8:c.1459T>A
|
ENSP00000295897.4:p.Leu487Met
|
|
ENST00000401494.7:c.1114T>A
|
ENSP00000384695.3:p.Leu372Met
|
|
ENST00000415165.6:c.883T>A
|
ENSP00000401820.2:p.Leu295Met
|
|
ENST00000476441.6:c.*738T>A
|
ENSP00000423727.1:n.*738T>A
|
|
ENST00000486939.1:n.113T>A
|
|
|
ENST00000503124.5:c.1009T>A
|
ENSP00000421027.1:p.Leu337Met
|
|
ENST00000505649.5:n.1006T>A
|
|
|
ENST00000509063.5:c.1459T>A
|
ENSP00000422784.1:p.Leu487Met
|
|
ENST00000511370.1:c.992T>A
|
|
|
ENST00000621085.4:c.820T>A
|
ENSP00000483421.1:p.Leu274Met
|
|
ENST00000621628.4:c.820T>A
|
ENSP00000480485.1:p.Leu274Met
|
|
NM_000477.5:c.1459T>A
|
NP_000468.1:p.Leu487Met
|
|
NM_000477.6:c.1459T>A
|
NP_000468.1:p.Leu487Met
|
|
NM_000477.7:c.1459T>A
MANE Select
|
NP_000468.1:p.Leu487Met
|
|