ENST00000396705.10:c.514G>T
MANE Select
|
ENSP00000379933.4:p.Gly172Cys
|
|
ENST00000229270.8:c.625G>T
|
ENSP00000229270.4:p.Gly209Cys
|
|
ENST00000396705.9:c.514G>T
|
ENSP00000379933.4:p.Gly172Cys
|
|
ENST00000482209.1:n.197G>T
|
|
|
ENST00000488464.6:c.268G>T
|
ENSP00000475620.1:p.Gly90Cys
|
|
ENST00000493987.5:c.268G>T
|
ENSP00000475364.1:p.Gly90Cys
|
|
ENST00000495834.1:c.268G>T
|
ENSP00000475829.1:p.Gly90Cys
|
|
ENST00000535434.5:c.268G>T
|
ENSP00000443599.1:p.Gly90Cys
|
|
ENST00000613953.4:c.625G>T
|
ENSP00000484435.1:p.Gly209Cys
|
|
NM_000365.5:c.514G>T
|
NP_000356.1:p.Gly172Cys
|
|
NM_001159287.1:c.625G>T
|
NP_001152759.1:p.Gly209Cys
|
|
NM_001258026.1:c.268G>T
|
NP_001244955.1:p.Gly90Cys
|
|
XR_002957378.1:n.1247G>T
|
|
|
NM_000365.6:c.514G>T
MANE Select
|
NP_000356.1:p.Gly172Cys
|
|
NM_001258026.2:c.268G>T
|
NP_001244955.1:p.Gly90Cys
|
|