ENST00000256646.7:c.1308G>T
MANE Select
|
ENSP00000256646.2:p.Thr436=
|
|
ENST00000640021.1:c.528G>T
|
ENSP00000492223.1:n.528G>T
|
|
ENST00000256646.6:c.1308G>T
|
ENSP00000256646.2:p.Thr436=
|
|
ENST00000479412.2:n.1446G>T
|
|
|
ENST00000579475.7:c.1191G>T
|
ENSP00000477065.2:p.Thr397=
|
|
NM_001200001.1:c.1308G>T
|
NP_001186930.1:p.Thr436=
|
|
NM_024408.3:c.1308G>T
|
NP_077719.2:p.Thr436=
|
|
XM_005270901.2:c.1191G>T
|
XP_005270958.1:p.Thr397=
|
|
XM_011541519.1:c.1296G>T
|
XP_011539821.1:p.Thr432=
|
|
XM_011541520.1:c.1191G>T
|
XP_011539822.1:p.Thr397=
|
|
NM_024408.4:c.1308G>T
MANE Select
|
NP_077719.2:p.Thr436=
|
|
NM_001200001.2:c.1308G>T
|
NP_001186930.1:p.Thr436=
|
|