ENST00000700555.2:n.640T>A
|
|
|
ENST00000700557.2:n.229T>A
|
|
|
ENST00000700559.2:c.2137T>A
|
ENSP00000515065.2:p.Ser713Thr
|
|
ENST00000546498.2:n.824T>A
|
|
|
ENST00000549461.2:n.659+17T>A
|
|
|
ENST00000700555.1:c.568T>A
|
ENSP00000515062.1:p.Ser190Thr
|
|
ENST00000700556.1:c.608T>A
|
|
|
ENST00000700557.1:c.148T>A
|
ENSP00000515064.1:p.Ser50Thr
|
|
ENST00000700558.1:n.351T>A
|
|
|
ENST00000700559.1:c.1352T>A
|
|
|
ENST00000700560.1:n.1352T>A
|
|
|
ENST00000700561.1:n.1478T>A
|
|
|
ENST00000070846.11:c.2269T>A
|
ENSP00000070846.6:p.Ser757Thr
|
|
ENST00000340811.9:c.2137T>A
MANE Select
|
ENSP00000342800.5:p.Ser713Thr
|
|
ENST00000070846.10:c.2269T>A
|
ENSP00000070846.6:p.Ser757Thr
|
|
ENST00000340811.8:c.2137T>A
|
ENSP00000342800.4:p.Ser713Thr
|
|
ENST00000613243.1:c.2269T>A
|
ENSP00000478295.1:p.Ser757Thr
|
|
NM_001005242.2:c.2137T>A
|
NP_001005242.2:p.Ser713Thr
|
|
NM_004572.3:c.2269T>A , LRG_398t1:c.2269T>A
|
NP_004563.2:p.Ser757Thr
|
|
NM_001005242.3:c.2137T>A
MANE Select
|
NP_001005242.2:p.Ser713Thr
|
|
NM_004572.4:c.2269T>A
|
NP_004563.2:p.Ser757Thr
|
|