ENST00000696502.1:c.4221G>A
|
ENSP00000512668.1:p.Ser1407=
|
|
ENST00000696503.1:c.4083G>A
|
ENSP00000512669.1:p.Ser1361=
|
|
ENST00000696504.1:c.4083G>A
|
ENSP00000512670.1:p.Ser1361=
|
|
ENST00000676179.1:c.4158G>A
MANE Select
|
ENSP00000502065.1:p.Ser1386=
|
|
ENST00000263934.10:c.4020G>A
|
ENSP00000263934.6:p.Ser1340=
|
|
ENST00000377081.5:c.4158G>A
|
ENSP00000366284.1:p.Ser1386=
|
|
ENST00000377086.5:c.4158G>A
|
ENSP00000366290.1:p.Ser1386=
|
|
ENST00000465635.5:n.613G>A
|
|
|
ENST00000483340.1:n.694G>A
|
|
|
ENST00000620295.2:c.4116G>A
|
ENSP00000478500.1:p.Ser1372=
|
|
ENST00000622724.3:c.4080G>A
|
ENSP00000480063.1:p.Ser1360=
|
|
ENST00000635499.1:c.203G>A
|
|
|
NM_015074.3:c.4020G>A , LRG_252t1:c.4020G>A
|
NP_055889.2:p.Ser1340=
|
|
XR_946953.1:n.401+390C>T
|
|
|
NM_001365951.1:c.4158G>A
|
NP_001352880.1:p.Ser1386=
|
|
NM_001365952.1:c.4158G>A
|
NP_001352881.1:p.Ser1386=
|
|
XR_946953.2:n.276+390C>T
|
|
|
NM_001365951.3:c.4158G>A
MANE Select
|
NP_001352880.1:p.Ser1386=
|
|