ENST00000295897.9:c.1120G>T
MANE Select
|
ENSP00000295897.4:p.Ala374Ser
|
|
ENST00000295897.8:c.1120G>T
|
ENSP00000295897.4:p.Ala374Ser
|
|
ENST00000401494.7:c.775G>T
|
ENSP00000384695.3:p.Ala259Ser
|
|
ENST00000415165.6:c.544G>T
|
ENSP00000401820.2:p.Ala182Ser
|
|
ENST00000476441.6:c.*399G>T
|
ENSP00000423727.1:n.*399G>T
|
|
ENST00000484992.1:n.440G>T
|
|
|
ENST00000503124.5:c.670G>T
|
ENSP00000421027.1:p.Ala224Ser
|
|
ENST00000504043.1:n.123G>T
|
|
|
ENST00000505649.5:n.806G>T
|
|
|
ENST00000509063.5:c.1120G>T
|
ENSP00000422784.1:p.Ala374Ser
|
|
ENST00000511370.1:c.653G>T
|
|
|
ENST00000621085.4:c.491-10G>T
|
ENSP00000483421.1:n.491-10G>T
|
|
ENST00000621628.4:c.487-6G>T
|
ENSP00000480485.1:n.487-6G>T
|
|
NM_000477.5:c.1120G>T
|
NP_000468.1:p.Ala374Ser
|
|
NM_000477.6:c.1120G>T
|
NP_000468.1:p.Ala374Ser
|
|
NM_000477.7:c.1120G>T
MANE Select
|
NP_000468.1:p.Ala374Ser
|
|