ENST00000268314.9:c.936C>T
MANE Select
|
ENSP00000268314.4:p.Gly312=
|
|
ENST00000268314.8:c.936C>T
|
ENSP00000268314.4:p.Gly312=
|
|
ENST00000408912.7:c.1221C>T
|
ENSP00000386125.3:p.Gly407=
|
|
ENST00000457010.6:c.936C>T
|
ENSP00000399561.2:p.Gly312=
|
|
ENST00000538189.5:c.444C>T
|
ENSP00000443995.2:p.Gly148=
|
|
ENST00000563544.5:c.936C>T
|
ENSP00000456877.1:p.Gly312=
|
|
ENST00000564900.1:c.213-289C>T
|
|
|
NM_001105247.1:c.936C>T
|
NP_001098717.1:p.Gly312=
|
|
NM_001288767.1:c.1221C>T
|
NP_001275696.1:p.Gly407=
|
|
NM_001301820.1:c.1032C>T
|
NP_001288749.1:p.Gly344=
|
|
NM_024742.2:c.936C>T
|
NP_079018.1:p.Gly312=
|
|
XM_006721091.1:c.1032C>T
|
XP_006721154.1:p.Gly344=
|
|
XM_006721091.3:c.1032C>T
|
XP_006721154.1:p.Gly344=
|
|
XM_024450448.1:c.1032C>T
|
XP_024306216.1:p.Gly344=
|
|
XM_024450449.1:c.1032C>T
|
XP_024306217.1:p.Gly344=
|
|
NM_001105247.2:c.936C>T
MANE Select
|
NP_001098717.1:p.Gly312=
|
|
NM_001288767.2:c.1221C>T
|
NP_001275696.1:p.Gly407=
|
|