ENST00000269980.7:c.1305G>T
MANE Select
|
ENSP00000269980.2:p.Gly435=
|
|
ENST00000269980.6:c.1305G>T
|
ENSP00000269980.2:p.Gly435=
|
|
ENST00000457836.6:c.1314G>T
|
ENSP00000416000.2:p.Gly438=
|
|
ENST00000540732.3:c.1407G>T
|
ENSP00000443246.1:p.Gly469=
|
|
ENST00000544905.1:c.135G>T
|
|
|
ENST00000595085.5:c.922+1878G>T
|
ENSP00000471150.2:n.922+1878G>T
|
|
NM_000709.3:c.1305G>T
|
NP_000700.1:p.Gly435=
|
|
NM_001164783.1:c.1302G>T
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NP_001158255.1:p.Gly434=
|
|
NM_000709.4:c.1305G>T
MANE Select
|
NP_000700.1:p.Gly435=
|
|
NM_001164783.2:c.1302G>T
|
NP_001158255.1:p.Gly434=
|
|