|
NM_006083.4:c.16+122A>G
MANE Select
|
NP_006074.2:n.16+122A>G
|
|
ENST00000417647.7:c.16+122A>G
MANE Select
|
ENSP00000396301.2:n.16+122A>G
|
|
NM_006083.3:c.16+122A>G
|
NP_006074.2:n.16+122A>G
|
|
ENST00000417647.6:c.16+122A>G
|
ENSP00000396301.2:n.16+122A>G
|
|
ENST00000503332.5:c.16+122A>G
|
ENSP00000421930.1:n.16+122A>G
|
|
ENST00000507593.5:c.16+122A>G
|
ENSP00000424622.1:n.16+122A>G
|
|
ENST00000508301.5:c.16+122A>G
|
ENSP00000422641.1:n.16+122A>G
|
|
ENST00000513256.5:c.5-425A>G
|
ENSP00000425564.1:n.5-425A>G
|
|
ENST00000523672.1:n.80+39A>G
|
|
|
ENST00000620556.4:c.16+122A>G
|
ENSP00000480993.1:n.16+122A>G
|
|
XR_002956156.1:n.107+122A>G
|
|