ENST00000513939.6:c.1082A>T
|
ENSP00000424211.2:p.Glu361Val
|
|
ENST00000616923.5:c.1037A>T
|
ENSP00000482756.2:p.Glu346Val
|
|
ENST00000643939.1:c.1202A>T
|
ENSP00000495686.1:p.Glu401Val
|
|
ENST00000650454.1:c.1196A>T
MANE Select
|
ENSP00000497574.1:p.Glu399Val
|
|
ENST00000229416.10:c.1196A>T
|
ENSP00000229416.6:p.Glu399Val
|
|
ENST00000504353.1:n.165A>T
|
|
|
ENST00000509541.5:n.1641A>T
|
|
|
ENST00000616923.4:c.1082A>T
|
ENSP00000482756.1:p.Glu361Val
|
|
NM_001197115.1:c.1082A>T
|
NP_001184044.1:p.Glu361Val
|
|
NM_001498.3:c.1196A>T
|
NP_001489.1:p.Glu399Val
|
|
NM_001498.4:c.1196A>T
MANE Select
|
NP_001489.1:p.Glu399Val
|
|
XM_017010749.1:c.485A>T
|
XP_016866238.1:p.Glu162Val
|
|
NM_001197115.2:c.1082A>T
|
NP_001184044.1:p.Glu361Val
|
|