ENST00000696502.1:c.4644C>T
|
ENSP00000512668.1:p.Ser1548=
|
|
ENST00000696503.1:c.4506C>T
|
ENSP00000512669.1:p.Ser1502=
|
|
ENST00000696504.1:c.4506C>T
|
ENSP00000512670.1:p.Ser1502=
|
|
ENST00000676179.1:c.4581C>T
MANE Select
|
ENSP00000502065.1:p.Ser1527=
|
|
ENST00000263934.10:c.4443C>T
|
ENSP00000263934.6:p.Ser1481=
|
|
ENST00000377081.5:c.4581C>T
|
ENSP00000366284.1:p.Ser1527=
|
|
ENST00000377086.5:c.4581C>T
|
ENSP00000366290.1:p.Ser1527=
|
|
ENST00000470616.1:n.312C>T
|
|
|
ENST00000620295.2:c.4539C>T
|
ENSP00000478500.1:p.Ser1513=
|
|
ENST00000622724.3:c.4503C>T
|
ENSP00000480063.1:p.Ser1501=
|
|
ENST00000635499.1:c.626C>T
|
|
|
NM_015074.3:c.4443C>T , LRG_252t1:c.4443C>T
|
NP_055889.2:p.Ser1481=
|
|
XR_946953.1:n.355+904G>A
|
|
|
NM_001365951.1:c.4581C>T
|
NP_001352880.1:p.Ser1527=
|
|
NM_001365952.1:c.4581C>T
|
NP_001352881.1:p.Ser1527=
|
|
XR_946953.2:n.230+904G>A
|
|
|
NM_001365951.3:c.4581C>T
MANE Select
|
NP_001352880.1:p.Ser1527=
|
|