ENST00000295897.9:c.1126A>T
MANE Select
|
ENSP00000295897.4:p.Thr376Ser
|
|
ENST00000295897.8:c.1126A>T
|
ENSP00000295897.4:p.Thr376Ser
|
|
ENST00000401494.7:c.781A>T
|
ENSP00000384695.3:p.Thr261Ser
|
|
ENST00000415165.6:c.550A>T
|
ENSP00000401820.2:p.Thr184Ser
|
|
ENST00000476441.6:c.*405A>T
|
ENSP00000423727.1:n.*405A>T
|
|
ENST00000484992.1:n.446A>T
|
|
|
ENST00000503124.5:c.676A>T
|
ENSP00000421027.1:p.Thr226Ser
|
|
ENST00000504043.1:n.129A>T
|
|
|
ENST00000505649.5:n.812A>T
|
|
|
ENST00000509063.5:c.1126A>T
|
ENSP00000422784.1:p.Thr376Ser
|
|
ENST00000511370.1:c.659A>T
|
|
|
ENST00000621085.4:c.491-4A>T
|
ENSP00000483421.1:n.491-4A>T
|
|
ENST00000621628.4:c.487A>T
|
ENSP00000480485.1:p.Thr163Ser
|
|
NM_000477.5:c.1126A>T
|
NP_000468.1:p.Thr376Ser
|
|
NM_000477.6:c.1126A>T
|
NP_000468.1:p.Thr376Ser
|
|
NM_000477.7:c.1126A>T
MANE Select
|
NP_000468.1:p.Thr376Ser
|
|