ENST00000295897.9:c.1610T>A
MANE Select
|
ENSP00000295897.4:p.Ile537Lys
|
|
ENST00000295897.8:c.1610T>A
|
ENSP00000295897.4:p.Ile537Lys
|
|
ENST00000401494.7:c.1265T>A
|
ENSP00000384695.3:p.Ile422Lys
|
|
ENST00000415165.6:c.1034T>A
|
ENSP00000401820.2:p.Ile345Lys
|
|
ENST00000476441.6:c.*889T>A
|
ENSP00000423727.1:n.*889T>A
|
|
ENST00000486939.1:n.264T>A
|
|
|
ENST00000503124.5:c.1160T>A
|
ENSP00000421027.1:p.Ile387Lys
|
|
ENST00000505649.5:n.1157T>A
|
|
|
ENST00000509063.5:c.1610T>A
|
ENSP00000422784.1:p.Ile537Lys
|
|
ENST00000511370.1:c.1143T>A
|
|
|
ENST00000621085.4:c.971T>A
|
ENSP00000483421.1:p.Ile324Lys
|
|
ENST00000621628.4:c.971T>A
|
ENSP00000480485.1:p.Ile324Lys
|
|
NM_000477.5:c.1610T>A
|
NP_000468.1:p.Ile537Lys
|
|
NM_000477.6:c.1610T>A
|
NP_000468.1:p.Ile537Lys
|
|
NM_000477.7:c.1610T>A
MANE Select
|
NP_000468.1:p.Ile537Lys
|
|