ENST00000295897.9:c.1131T>G
MANE Select
|
ENSP00000295897.4:p.Tyr377Ter
|
|
ENST00000295897.8:c.1131T>G
|
ENSP00000295897.4:p.Tyr377Ter
|
|
ENST00000401494.7:c.786T>G
|
ENSP00000384695.3:p.Tyr262Ter
|
|
ENST00000415165.6:c.555T>G
|
ENSP00000401820.2:p.Tyr185Ter
|
|
ENST00000476441.6:c.*410T>G
|
ENSP00000423727.1:n.*410T>G
|
|
ENST00000484992.1:n.451T>G
|
|
|
ENST00000503124.5:c.681T>G
|
ENSP00000421027.1:p.Tyr227Ter
|
|
ENST00000504043.1:n.134T>G
|
|
|
ENST00000505649.5:n.817T>G
|
|
|
ENST00000509063.5:c.1131T>G
|
ENSP00000422784.1:p.Tyr377Ter
|
|
ENST00000511370.1:c.664T>G
|
|
|
ENST00000621085.4:c.492T>G
|
ENSP00000483421.1:p.Tyr164Ter
|
|
ENST00000621628.4:c.492T>G
|
ENSP00000480485.1:p.Tyr164Ter
|
|
NM_000477.5:c.1131T>G
|
NP_000468.1:p.Tyr377Ter
|
|
NM_000477.6:c.1131T>G
|
NP_000468.1:p.Tyr377Ter
|
|
NM_000477.7:c.1131T>G
MANE Select
|
NP_000468.1:p.Tyr377Ter
|
|