ENST00000261304.7:c.1459C>A
MANE Select
|
ENSP00000261304.2:p.Pro487Thr
|
|
ENST00000261304.6:c.1459C>A
|
ENSP00000261304.2:p.Pro487Thr
|
|
ENST00000393568.8:c.1390C>A
|
ENSP00000377198.4:p.Pro464Thr
|
|
ENST00000393569.6:c.1381C>A
|
ENSP00000377199.2:p.Pro461Thr
|
|
ENST00000544807.6:c.1291C>A
|
ENSP00000437513.2:p.Pro431Thr
|
|
ENST00000555000.5:c.826C>A
|
ENSP00000450472.1:p.Pro276Thr
|
|
ENST00000555179.1:c.176C>A
|
|
|
ENST00000557316.5:c.*857C>A
|
ENSP00000452314.1:n.*857C>A
|
|
NM_000153.3:c.1459C>A
|
NP_000144.2:p.Pro487Thr
|
|
NM_001201401.1:c.1390C>A
|
NP_001188330.1:p.Pro464Thr
|
|
NM_001201402.1:c.1381C>A
|
NP_001188331.1:p.Pro461Thr
|
|
XM_011536618.1:c.1291C>A
|
XP_011534920.1:p.Pro431Thr
|
|
XM_011536618.2:c.1291C>A
|
XP_011534920.1:p.Pro431Thr
|
|
NM_000153.4:c.1459C>A
MANE Select
|
NP_000144.2:p.Pro487Thr
|
|
NM_001201401.2:c.1390C>A
|
NP_001188330.1:p.Pro464Thr
|
|
NM_001201402.2:c.1381C>A
|
NP_001188331.1:p.Pro461Thr
|
|