ENST00000247026.10:c.20+212G>T
MANE Select
|
ENSP00000247026.5:n.20+212G>T
|
|
ENST00000247026.9:c.20+212G>T
|
ENSP00000247026.5:n.20+212G>T
|
|
ENST00000394826.8:c.20+212G>T
|
ENSP00000378303.4:n.20+212G>T
|
|
ENST00000475652.5:c.20+212G>T
|
ENSP00000464569.1:n.20+212G>T
|
|
ENST00000479218.6:c.20+212G>T
|
ENSP00000466640.1:n.20+212G>T
|
|
ENST00000540900.7:n.321+212G>T
|
|
|
ENST00000577289.6:n.45+212G>T
|
|
|
ENST00000583301.5:n.25+212G>T
|
|
|
ENST00000584154.5:c.20+212G>T
|
ENSP00000462820.1:n.20+212G>T
|
|
ENST00000584317.5:c.20+212G>T
|
ENSP00000463722.1:n.20+212G>T
|
|
ENST00000584423.5:c.20+212G>T
|
ENSP00000464237.1:n.20+212G>T
|
|
ENST00000585881.5:c.-306G>T
|
ENSP00000465442.1:n.-306G>T
|
|
ENST00000612959.4:c.-49+212G>T
|
ENSP00000477862.1:n.-49+212G>T
|
|
NM_001261467.1:c.-49+212G>T
|
NP_001248396.1:n.-49+212G>T
|
|
NM_032141.3:c.20+212G>T
|
NP_115517.1:n.20+212G>T
|
|
XM_011525345.1:c.20+212G>T
|
XP_011523647.1:n.20+212G>T
|
|
XR_934651.1:n.682+317C>A
|
|
|
XM_011525345.2:c.20+212G>T
|
XP_011523647.1:n.20+212G>T
|
|
NM_032141.4:c.20+212G>T
MANE Select
|
NP_115517.1:n.20+212G>T
|
|
NM_001261467.2:c.-49+212G>T
|
NP_001248396.1:n.-49+212G>T
|
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