ENST00000465378.6:n.1077A>G
|
|
|
ENST00000642923.1:c.667+257A>G
|
ENSP00000494255.1:n.667+257A>G
|
|
ENST00000643137.1:c.667+257A>G
|
ENSP00000495331.1:n.667+257A>G
|
|
ENST00000644006.1:c.*216+257A>G
|
ENSP00000493778.1:n.*216+257A>G
|
|
ENST00000645026.1:n.823+257A>G
|
|
|
ENST00000645190.1:c.772+257A>G
MANE Select
|
ENSP00000496496.1:n.772+257A>G
|
|
ENST00000647301.1:c.*216+257A>G
|
ENSP00000496641.1:n.*216+257A>G
|
|
ENST00000290846.8:c.772+257A>G
|
ENSP00000290846.4:n.772+257A>G
|
|
ENST00000381019.3:c.772+257A>G
|
ENSP00000370407.3:n.772+257A>G
|
|
ENST00000381021.7:c.*365+257A>G
|
ENSP00000370409.3:n.*365+257A>G
|
|
ENST00000441818.5:c.*306+257A>G
|
ENSP00000393014.1:n.*306+257A>G
|
|
ENST00000453630.5:c.*310+257A>G
|
ENSP00000398488.1:n.*310+257A>G
|
|
ENST00000456595.5:c.*306+257A>G
|
ENSP00000413880.1:n.*306+257A>G
|
|
ENST00000457572.5:c.*216+257A>G
|
ENSP00000407700.1:n.*216+257A>G
|
|
ENST00000463785.1:n.303A>G
|
|
|
NM_001282782.1:c.430+257A>G
|
NP_001269711.1:n.430+257A>G
|
|
NM_001282783.1:c.352+257A>G
|
NP_001269712.1:n.352+257A>G
|
|
NM_001282784.1:c.352+257A>G
|
NP_001269713.1:n.352+257A>G
|
|
NM_001282785.1:c.772+257A>G
|
NP_001269714.1:n.772+257A>G
|
|
NM_018006.4:c.772+257A>G
|
NP_060476.2:n.772+257A>G
|
|
NR_104240.1:n.1081+257A>G
|
|
|
NR_104241.1:n.974+257A>G
|
|
|
XM_005261678.1:c.376+257A>G
|
XP_005261735.1:n.376+257A>G
|
|
XM_005261681.1:c.376+257A>G
|
XP_005261738.1:n.376+257A>G
|
|
XM_011530271.1:c.667+257A>G
|
XP_011528573.1:n.667+257A>G
|
|
XM_011530272.1:c.772+257A>G
|
XP_011528574.1:n.772+257A>G
|
|
XM_011530273.1:c.772+257A>G
|
XP_011528575.1:n.772+257A>G
|
|
XM_011530274.1:c.430+257A>G
|
XP_011528576.1:n.430+257A>G
|
|
XM_011530275.1:c.376+257A>G
|
XP_011528577.1:n.376+257A>G
|
|
XM_011530271.2:c.667+257A>G
|
XP_011528573.1:n.667+257A>G
|
|
XM_011530272.2:c.772+257A>G
|
XP_011528574.1:n.772+257A>G
|
|
XM_011530273.2:c.772+257A>G
|
XP_011528575.1:n.772+257A>G
|
|
XM_011530274.2:c.430+257A>G
|
XP_011528576.1:n.430+257A>G
|
|
XM_024452260.1:c.667+257A>G
|
XP_024308028.1:n.667+257A>G
|
|
XR_001755261.2:n.881A>G
|
|
|
XR_001755262.2:n.881A>G
|
|
|
NM_018006.5:c.772+257A>G
MANE Select
|
NP_060476.2:n.772+257A>G
|
|
NM_001282782.2:c.430+257A>G
|
NP_001269711.1:n.430+257A>G
|
|
NM_001282783.2:c.352+257A>G
|
NP_001269712.1:n.352+257A>G
|
|
NM_001282784.2:c.352+257A>G
|
NP_001269713.1:n.352+257A>G
|
|
NM_001282785.2:c.772+257A>G
|
NP_001269714.1:n.772+257A>G
|
|
NR_104240.2:n.768+257A>G
|
|
|
NR_104241.2:n.661+257A>G
|
|
|