ENST00000295897.9:c.1804G>T
MANE Select
|
ENSP00000295897.4:p.Ala602Ser
|
|
ENST00000295897.8:c.1804G>T
|
ENSP00000295897.4:p.Ala602Ser
|
|
ENST00000401494.7:c.1459G>T
|
ENSP00000384695.3:p.Ala487Ser
|
|
ENST00000415165.6:c.1228G>T
|
ENSP00000401820.2:p.Ala410Ser
|
|
ENST00000476441.6:c.*1083G>T
|
ENSP00000423727.1:n.*1083G>T
|
|
ENST00000495173.1:n.112G>T
|
|
|
ENST00000503124.5:c.1354G>T
|
ENSP00000421027.1:p.Ala452Ser
|
|
ENST00000505649.5:n.1351G>T
|
|
|
ENST00000508932.5:n.194G>T
|
|
|
ENST00000509063.5:c.1785+633G>T
|
ENSP00000422784.1:n.1785+633G>T
|
|
ENST00000511370.1:c.1337G>T
|
|
|
ENST00000621085.4:c.1165G>T
|
ENSP00000483421.1:p.Ala389Ser
|
|
ENST00000621628.4:c.1165G>T
|
ENSP00000480485.1:p.Ala389Ser
|
|
NM_000477.5:c.1804G>T
|
NP_000468.1:p.Ala602Ser
|
|
NM_000477.6:c.1804G>T
|
NP_000468.1:p.Ala602Ser
|
|
NM_000477.7:c.1804G>T
MANE Select
|
NP_000468.1:p.Ala602Ser
|
|