ENST00000698508.1:c.1342G>T
|
ENSP00000513759.1:p.Gly448Trp
|
|
ENST00000698509.1:n.1482G>T
|
|
|
ENST00000264972.10:c.1342G>T
MANE Select
|
ENSP00000264972.5:p.Gly448Trp
|
|
ENST00000264972.9:c.1342G>T
|
ENSP00000264972.5:p.Gly448Trp
|
|
ENST00000451498.2:c.421G>T
|
ENSP00000400475.2:p.Gly141Trp
|
|
ENST00000463643.5:n.1203G>T
|
|
|
ENST00000487283.5:n.2394G>T
|
|
|
ENST00000495754.1:n.280G>T
|
|
|
NM_001079.3:c.1342G>T , LRG_126t1:c.1342G>T
|
NP_001070.2:p.Gly448Trp
|
|
NM_207519.1:c.421G>T
|
NP_997402.1:p.Gly141Trp
|
|
XM_005264015.3:c.1324G>T
|
XP_005264072.1:p.Gly442Trp
|
|
XM_006712728.2:c.1342G>T
|
XP_006712791.1:p.Gly448Trp
|
|
XM_011511783.1:c.1342G>T
|
XP_011510085.1:p.Gly448Trp
|
|
XR_923018.1:n.1544G>T
|
|
|
XR_923019.1:n.1544G>T
|
|
|
XR_923020.1:n.1544G>T
|
|
|
XM_017004867.1:c.1711G>T
|
XP_016860356.1:p.Gly571Trp
|
|
XM_017004868.1:c.1693G>T
|
XP_016860357.1:p.Gly565Trp
|
|
XM_017004869.1:c.1711G>T
|
XP_016860358.1:p.Gly571Trp
|
|
XM_017004870.1:c.1711G>T
|
XP_016860359.1:p.Gly571Trp
|
|
XR_001738925.1:n.2950G>T
|
|
|
XR_001738926.1:n.2950G>T
|
|
|
XR_001738927.1:n.2950G>T
|
|
|
NM_001079.4:c.1342G>T
MANE Select
|
NP_001070.2:p.Gly448Trp
|
|
NM_001378594.1:c.1342G>T
|
NP_001365523.1:p.Gly448Trp
|
|
NM_207519.2:c.421G>T
|
NP_997402.1:p.Gly141Trp
|
|