|
NM_025074.7:c.9316+2T>A
MANE Select
|
NP_079350.5:n.9316+2T>A
|
|
ENST00000512123.4:c.9316+2T>A
MANE Select
|
ENSP00000422834.2:n.9316+2T>A
|
|
NM_025074.6:c.9316+2T>A
|
NP_079350.5:n.9316+2T>A
|
|
ENST00000512123.3:c.9316+2T>A
|
ENSP00000422834.2:n.9316+2T>A
|
|
ENST00000682513.1:c.9316+2T>A
|
ENSP00000508201.1:n.9316+2T>A
|
|
XM_006714314.1:c.9310+2T>A
|
XP_006714377.1:n.9310+2T>A
|
|
XM_006714316.1:c.9088+2T>A
|
XP_006714379.1:n.9088+2T>A
|
|
XM_006714316.3:c.9088+2T>A
|
XP_006714379.1:n.9088+2T>A
|
|
XM_011532270.1:c.7015+2T>A
|
XP_011530572.1:n.7015+2T>A
|
|
XM_011532271.1:c.4204+2T>A
|
XP_011530573.1:n.4204+2T>A
|