ENST00000295897.9:c.1708G>T
MANE Select
|
ENSP00000295897.4:p.Ala570Ser
|
|
ENST00000295897.8:c.1708G>T
|
ENSP00000295897.4:p.Ala570Ser
|
|
ENST00000401494.7:c.1363G>T
|
ENSP00000384695.3:p.Ala455Ser
|
|
ENST00000415165.6:c.1132G>T
|
ENSP00000401820.2:p.Ala378Ser
|
|
ENST00000476441.6:c.*987G>T
|
ENSP00000423727.1:n.*987G>T
|
|
ENST00000495173.1:n.16G>T
|
|
|
ENST00000503124.5:c.1258G>T
|
ENSP00000421027.1:p.Ala420Ser
|
|
ENST00000505649.5:n.1255G>T
|
|
|
ENST00000508932.5:n.175+107G>T
|
|
|
ENST00000509063.5:c.1708G>T
|
ENSP00000422784.1:p.Ala570Ser
|
|
ENST00000511370.1:c.1241G>T
|
|
|
ENST00000621085.4:c.1069G>T
|
ENSP00000483421.1:p.Ala357Ser
|
|
ENST00000621628.4:c.1069G>T
|
ENSP00000480485.1:p.Ala357Ser
|
|
NM_000477.5:c.1708G>T
|
NP_000468.1:p.Ala570Ser
|
|
NM_000477.6:c.1708G>T
|
NP_000468.1:p.Ala570Ser
|
|
NM_000477.7:c.1708G>T
MANE Select
|
NP_000468.1:p.Ala570Ser
|
|