ENST00000295897.9:c.1685A>C
MANE Select
|
ENSP00000295897.4:p.Lys562Thr
|
|
ENST00000295897.8:c.1685A>C
|
ENSP00000295897.4:p.Lys562Thr
|
|
ENST00000401494.7:c.1340A>C
|
ENSP00000384695.3:p.Lys447Thr
|
|
ENST00000415165.6:c.1109A>C
|
ENSP00000401820.2:p.Lys370Thr
|
|
ENST00000476441.6:c.*964A>C
|
ENSP00000423727.1:n.*964A>C
|
|
ENST00000486939.1:n.339A>C
|
|
|
ENST00000503124.5:c.1235A>C
|
ENSP00000421027.1:p.Lys412Thr
|
|
ENST00000505649.5:n.1232A>C
|
|
|
ENST00000508932.5:n.175+84A>C
|
|
|
ENST00000509063.5:c.1685A>C
|
ENSP00000422784.1:p.Lys562Thr
|
|
ENST00000511370.1:c.1218A>C
|
|
|
ENST00000621085.4:c.1046A>C
|
ENSP00000483421.1:p.Lys349Thr
|
|
ENST00000621628.4:c.1046A>C
|
ENSP00000480485.1:p.Lys349Thr
|
|
NM_000477.5:c.1685A>C
|
NP_000468.1:p.Lys562Thr
|
|
NM_000477.6:c.1685A>C
|
NP_000468.1:p.Lys562Thr
|
|
NM_000477.7:c.1685A>C
MANE Select
|
NP_000468.1:p.Lys562Thr
|
|