ENST00000178640.10:c.1243-3899G>A
MANE Select
|
ENSP00000178640.5:n.1243-3899G>A
|
|
ENST00000178640.9:c.1243-3899G>A
|
ENSP00000178640.5:n.1243-3899G>A
|
|
ENST00000340972.8:c.673-3899G>A
|
ENSP00000342101.4:n.673-3899G>A
|
|
ENST00000354498.9:c.1135-3899G>A
|
ENSP00000346493.5:n.1135-3899G>A
|
|
ENST00000395476.6:c.1213-3899G>A
|
ENSP00000378859.2:n.1213-3899G>A
|
|
ENST00000558274.1:n.327-3899G>A
|
|
|
ENST00000558392.5:n.1069-3899G>A
|
|
|
NM_001206804.1:c.1135-3899G>A
|
NP_001193733.1:n.1135-3899G>A
|
|
NM_002757.3:c.1213-3899G>A
|
NP_002748.1:n.1213-3899G>A
|
|
NM_145160.2:c.1243-3899G>A
|
NP_660143.1:n.1243-3899G>A
|
|
XM_011521784.1:c.1288-3899G>A
|
XP_011520086.1:n.1288-3899G>A
|
|
XM_011521786.1:c.1216-3899G>A
|
XP_011520088.1:n.1216-3899G>A
|
|
XM_024449988.1:c.1012-3899G>A
|
XP_024305756.1:n.1012-3899G>A
|
|
NM_145160.3:c.1243-3899G>A
MANE Select
|
NP_660143.1:n.1243-3899G>A
|
|
NM_001206804.2:c.1135-3899G>A
|
NP_001193733.1:n.1135-3899G>A
|
|
NM_002757.4:c.1213-3899G>A
|
NP_002748.1:n.1213-3899G>A
|
|