ENST00000268314.9:c.1072G>T
MANE Select
|
ENSP00000268314.4:p.Glu358Ter
|
|
ENST00000268314.8:c.1072G>T
|
ENSP00000268314.4:p.Glu358Ter
|
|
ENST00000408912.7:c.1357G>T
|
ENSP00000386125.3:p.Glu453Ter
|
|
ENST00000457010.6:c.1072G>T
|
ENSP00000399561.2:p.Glu358Ter
|
|
ENST00000538189.5:c.580G>T
|
ENSP00000443995.2:p.Glu194Ter
|
|
ENST00000563544.5:c.1072G>T
|
ENSP00000456877.1:p.Glu358Ter
|
|
ENST00000564900.1:c.213-153G>T
|
|
|
NM_001105247.1:c.1072G>T
|
NP_001098717.1:p.Glu358Ter
|
|
NM_001288767.1:c.1357G>T
|
NP_001275696.1:p.Glu453Ter
|
|
NM_001301820.1:c.1168G>T
|
NP_001288749.1:p.Glu390Ter
|
|
NM_024742.2:c.1072G>T
|
NP_079018.1:p.Glu358Ter
|
|
XM_006721091.1:c.1168G>T
|
XP_006721154.1:p.Glu390Ter
|
|
XM_006721091.3:c.1168G>T
|
XP_006721154.1:p.Glu390Ter
|
|
XM_024450448.1:c.1168G>T
|
XP_024306216.1:p.Glu390Ter
|
|
XM_024450449.1:c.1168G>T
|
XP_024306217.1:p.Glu390Ter
|
|
NM_001105247.2:c.1072G>T
MANE Select
|
NP_001098717.1:p.Glu358Ter
|
|
NM_001288767.2:c.1357G>T
|
NP_001275696.1:p.Glu453Ter
|
|