ENST00000698508.1:c.1362G>T
|
ENSP00000513759.1:p.Glu454Asp
|
|
ENST00000698509.1:n.1502G>T
|
|
|
ENST00000264972.10:c.1362G>T
MANE Select
|
ENSP00000264972.5:p.Glu454Asp
|
|
ENST00000264972.9:c.1362G>T
|
ENSP00000264972.5:p.Glu454Asp
|
|
ENST00000451498.2:c.441G>T
|
ENSP00000400475.2:p.Glu147Asp
|
|
ENST00000463643.5:n.1223G>T
|
|
|
ENST00000487283.5:n.2414G>T
|
|
|
ENST00000495754.1:n.300G>T
|
|
|
NM_001079.3:c.1362G>T , LRG_126t1:c.1362G>T
|
NP_001070.2:p.Glu454Asp
|
|
NM_207519.1:c.441G>T
|
NP_997402.1:p.Glu147Asp
|
|
XM_005264015.3:c.1344G>T
|
XP_005264072.1:p.Glu448Asp
|
|
XM_006712728.2:c.1362G>T
|
XP_006712791.1:p.Glu454Asp
|
|
XM_011511783.1:c.1362G>T
|
XP_011510085.1:p.Glu454Asp
|
|
XR_923018.1:n.1564G>T
|
|
|
XR_923019.1:n.1564G>T
|
|
|
XR_923020.1:n.1564G>T
|
|
|
XM_017004867.1:c.1731G>T
|
XP_016860356.1:p.Glu577Asp
|
|
XM_017004868.1:c.1713G>T
|
XP_016860357.1:p.Glu571Asp
|
|
XM_017004869.1:c.1731G>T
|
XP_016860358.1:p.Glu577Asp
|
|
XM_017004870.1:c.1731G>T
|
XP_016860359.1:p.Glu577Asp
|
|
XR_001738925.1:n.2970G>T
|
|
|
XR_001738926.1:n.2970G>T
|
|
|
XR_001738927.1:n.2970G>T
|
|
|
NM_001079.4:c.1362G>T
MANE Select
|
NP_001070.2:p.Glu454Asp
|
|
NM_001378594.1:c.1362G>T
|
NP_001365523.1:p.Glu454Asp
|
|
NM_207519.2:c.441G>T
|
NP_997402.1:p.Glu147Asp
|
|