ENST00000327047.6:c.671C>G
MANE Select
|
ENSP00000322280.1:p.Thr224Ser
|
|
ENST00000295911.6:c.342+101C>G
|
ENSP00000295911.2:n.342+101C>G
|
|
ENST00000327047.5:c.671C>G
|
ENSP00000322280.1:p.Thr224Ser
|
|
ENST00000328863.8:c.710C>G
|
ENSP00000329158.4:p.Thr237Ser
|
|
ENST00000562308.5:c.104+13618C>G
|
|
|
ENST00000565169.1:c.162+13618C>G
|
|
|
ENST00000569170.5:c.162+13618C>G
|
|
|
NM_001195794.1:c.710C>G , LRG_700t1:c.710C>G
|
NP_001182723.1:p.Thr237Ser
|
|
NM_001256819.1:c.*285C>G
|
NP_001243748.1:n.*285C>G
|
|
NM_052995.2:c.342+101C>G , LRG_700t2:c.342+101C>G
|
NP_443721.1:n.342+101C>G
|
|
NM_174878.2:c.671C>G
|
NP_777367.1:p.Thr224Ser
|
|
NR_046380.2:n.1152C>G
|
|
|
XR_924167.1:n.983C>G
|
|
|
NM_001256819.2:c.*285C>G
|
NP_001243748.1:n.*285C>G
|
|
NM_174878.3:c.671C>G
MANE Select
|
NP_777367.1:p.Thr224Ser
|
|
NR_046380.3:n.880C>G
|
|
|