ENST00000698508.1:c.1741G>T
|
ENSP00000513759.1:p.Glu581Ter
|
|
ENST00000698509.1:n.1881G>T
|
|
|
ENST00000264972.10:c.1741G>T
MANE Select
|
ENSP00000264972.5:p.Glu581Ter
|
|
ENST00000264972.9:c.1741G>T
|
ENSP00000264972.5:p.Glu581Ter
|
|
ENST00000451498.2:c.820G>T
|
ENSP00000400475.2:p.Glu274Ter
|
|
ENST00000463643.5:n.1602G>T
|
|
|
ENST00000487283.5:n.2793G>T
|
|
|
NM_001079.3:c.1741G>T , LRG_126t1:c.1741G>T
|
NP_001070.2:p.Glu581Ter
|
|
NM_207519.1:c.820G>T
|
NP_997402.1:p.Glu274Ter
|
|
XM_005264015.3:c.1723G>T
|
XP_005264072.1:p.Glu575Ter
|
|
XM_011511783.1:c.1736+1272G>T
|
XP_011510085.1:n.1736+1272G>T
|
|
XR_923018.1:n.1938+1272G>T
|
|
|
XR_923019.1:n.1938+1272G>T
|
|
|
XR_923020.1:n.2152G>T
|
|
|
XM_017004867.1:c.2110G>T
|
XP_016860356.1:p.Glu704Ter
|
|
XM_017004868.1:c.2092G>T
|
XP_016860357.1:p.Glu698Ter
|
|
XM_017004869.1:c.2105+1272G>T
|
XP_016860358.1:n.2105+1272G>T
|
|
XR_001738925.1:n.3344+1272G>T
|
|
|
XR_001738926.1:n.3344+1272G>T
|
|
|
XR_001738927.1:n.3558G>T
|
|
|
NM_001079.4:c.1741G>T
MANE Select
|
NP_001070.2:p.Glu581Ter
|
|
NM_001378594.1:c.1741G>T
|
NP_001365523.1:p.Glu581Ter
|
|
NM_207519.2:c.820G>T
|
NP_997402.1:p.Glu274Ter
|
|