ENST00000295897.9:c.1129T>G
MANE Select
|
ENSP00000295897.4:p.Tyr377Asp
|
|
ENST00000295897.8:c.1129T>G
|
ENSP00000295897.4:p.Tyr377Asp
|
|
ENST00000401494.7:c.784T>G
|
ENSP00000384695.3:p.Tyr262Asp
|
|
ENST00000415165.6:c.553T>G
|
ENSP00000401820.2:p.Tyr185Asp
|
|
ENST00000476441.6:c.*408T>G
|
ENSP00000423727.1:n.*408T>G
|
|
ENST00000484992.1:n.449T>G
|
|
|
ENST00000503124.5:c.679T>G
|
ENSP00000421027.1:p.Tyr227Asp
|
|
ENST00000504043.1:n.132T>G
|
|
|
ENST00000505649.5:n.815T>G
|
|
|
ENST00000509063.5:c.1129T>G
|
ENSP00000422784.1:p.Tyr377Asp
|
|
ENST00000511370.1:c.662T>G
|
|
|
ENST00000621085.4:c.491-1T>G
|
ENSP00000483421.1:n.491-1T>G
|
|
ENST00000621628.4:c.490T>G
|
ENSP00000480485.1:p.Tyr164Asp
|
|
NM_000477.5:c.1129T>G
|
NP_000468.1:p.Tyr377Asp
|
|
NM_000477.6:c.1129T>G
|
NP_000468.1:p.Tyr377Asp
|
|
NM_000477.7:c.1129T>G
MANE Select
|
NP_000468.1:p.Tyr377Asp
|
|