ENST00000327047.6:c.433+894T>C
MANE Select
|
ENSP00000322280.1:n.433+894T>C
|
|
ENST00000468836.2:c.581+894T>C
|
ENSP00000419892.2:n.581+894T>C
|
|
ENST00000644099.1:c.426-169T>C
|
ENSP00000494762.1:n.426-169T>C
|
|
ENST00000295911.6:c.205+894T>C
|
ENSP00000295911.2:n.205+894T>C
|
|
ENST00000327047.5:c.433+894T>C
|
ENSP00000322280.1:n.433+894T>C
|
|
ENST00000328863.8:c.434-169T>C
|
ENSP00000329158.4:n.434-169T>C
|
|
ENST00000468836.1:c.205+894T>C
|
ENSP00000419892.1:n.205+894T>C
|
|
ENST00000485607.1:c.97+894T>C
|
ENSP00000419244.1:n.97+894T>C
|
|
ENST00000562308.5:c.104+894T>C
|
|
|
ENST00000565169.1:c.162+894T>C
|
|
|
ENST00000569170.5:c.162+894T>C
|
|
|
NM_001195794.1:c.434-169T>C , LRG_700t1:c.434-169T>C
|
NP_001182723.1:n.434-169T>C
|
|
NM_001256819.1:c.*47+894T>C
|
NP_001243748.1:n.*47+894T>C
|
|
NM_052995.2:c.205+894T>C , LRG_700t2:c.205+894T>C
|
NP_443721.1:n.205+894T>C
|
|
NM_174878.2:c.433+894T>C
|
NP_777367.1:n.433+894T>C
|
|
NR_046380.2:n.876-169T>C
|
|
|
XR_924167.1:n.745+894T>C
|
|
|
NM_001256819.2:c.*47+894T>C
|
NP_001243748.1:n.*47+894T>C
|
|
NM_174878.3:c.433+894T>C
MANE Select
|
NP_777367.1:n.433+894T>C
|
|
NR_046380.3:n.604-169T>C
|
|
|