ENST00000261304.7:c.229C>A
MANE Select
|
ENSP00000261304.2:p.Pro77Thr
|
|
ENST00000261304.6:c.229C>A
|
ENSP00000261304.2:p.Pro77Thr
|
|
ENST00000393568.8:c.196-283C>A
|
ENSP00000377198.4:n.196-283C>A
|
|
ENST00000393569.6:c.151C>A
|
ENSP00000377199.2:p.Pro51Thr
|
|
ENST00000474294.6:n.219C>A
|
|
|
ENST00000544807.6:c.61C>A
|
ENSP00000437513.2:p.Pro21Thr
|
|
ENST00000554372.5:c.229C>A
|
ENSP00000451884.1:p.Pro77Thr
|
|
ENST00000554916.5:n.108C>A
|
|
|
ENST00000555956.1:n.34C>A
|
|
|
ENST00000556879.5:c.289C>A
|
ENSP00000452208.1:n.289C>A
|
|
ENST00000557316.5:c.229C>A
|
ENSP00000452314.1:p.Pro77Thr
|
|
ENST00000622264.4:c.219C>A
|
|
|
NM_000153.3:c.229C>A
|
NP_000144.2:p.Pro77Thr
|
|
NM_001201401.1:c.196-283C>A
|
NP_001188330.1:n.196-283C>A
|
|
NM_001201402.1:c.151C>A
|
NP_001188331.1:p.Pro51Thr
|
|
XM_011536618.1:c.61C>A
|
XP_011534920.1:p.Pro21Thr
|
|
XM_011536618.2:c.61C>A
|
XP_011534920.1:p.Pro21Thr
|
|
NM_000153.4:c.229C>A
MANE Select
|
NP_000144.2:p.Pro77Thr
|
|
NM_001201401.2:c.196-283C>A
|
NP_001188330.1:n.196-283C>A
|
|
NM_001201402.2:c.151C>A
|
NP_001188331.1:p.Pro51Thr
|
|