ENST00000477616.2:c.2170+8G>A
MANE Select
|
ENSP00000434241.1:n.2170+8G>A
|
|
ENST00000670667.1:c.2170+8G>A
|
ENSP00000499301.1:n.2170+8G>A
|
|
ENST00000376959.6:c.2170+8G>A
|
ENSP00000366158.2:n.2170+8G>A
|
|
ENST00000474951.1:c.118+8G>A
|
ENSP00000432438.1:n.118+8G>A
|
|
ENST00000477616.1:c.2170+8G>A
|
ENSP00000434241.1:n.2170+8G>A
|
|
NM_004977.2:c.2170+8G>A
|
NP_004968.2:n.2170+8G>A
|
|
NR_110912.1:n.239+8G>A
|
|
|
XM_006723203.2:c.2170+8G>A
|
XP_006723266.1:n.2170+8G>A
|
|
XM_011526925.1:c.2170+8G>A
|
XP_011525227.1:n.2170+8G>A
|
|
XM_011526926.1:c.2170+8G>A
|
XP_011525228.1:n.2170+8G>A
|
|
XM_011526927.1:c.2170+8G>A
|
XP_011525229.1:n.2170+8G>A
|
|
XM_011526928.1:c.2170+8G>A
|
XP_011525230.1:n.2170+8G>A
|
|
NM_001372305.1:c.1942+8G>A
|
NP_001359234.1:n.1942+8G>A
|
|
NM_004977.3:c.2170+8G>A
MANE Select
|
NP_004968.2:n.2170+8G>A
|
|
NR_110912.2:n.260+8G>A
|
|
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