ENST00000408954.8:c.62+41249G>A
MANE Select
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ENSP00000386135.3:n.62+41249G>A
|
|
ENST00000358077.9:c.62+41249G>A
|
ENSP00000350785.5:n.62+41249G>A
|
|
ENST00000408954.7:c.62+41249G>A
|
ENSP00000386135.3:n.62+41249G>A
|
|
ENST00000469067.5:n.542+41249G>A
|
|
|
ENST00000469640.6:c.62+41249G>A
|
ENSP00000418885.3:n.62+41249G>A
|
|
ENST00000472284.5:c.62+41249G>A
|
ENSP00000417076.1:n.62+41249G>A
|
|
ENST00000472344.1:n.196+41249G>A
|
|
|
ENST00000489291.5:c.62+41249G>A
|
ENSP00000417746.1:n.62+41249G>A
|
|
ENST00000491893.5:c.62+41249G>A
|
ENSP00000419026.1:n.62+41249G>A
|
|
ENST00000496522.5:n.272+41249G>A
|
|
|
ENST00000622514.4:c.62+41249G>A
|
ENSP00000484267.1:n.62+41249G>A
|
|
NM_001288729.1:c.62+41249G>A
|
NP_001275658.1:n.62+41249G>A
|
|
NM_001288730.1:c.62+41249G>A
|
NP_001275659.1:n.62+41249G>A
|
|
NM_001288731.1:c.62+41249G>A
|
NP_001275660.1:n.62+41249G>A
|
|
NM_004938.3:c.62+41249G>A
|
NP_004929.2:n.62+41249G>A
|
|
XM_005251757.2:c.62+41249G>A
|
XP_005251814.1:n.62+41249G>A
|
|
XM_005251757.4:c.62+41249G>A
|
XP_005251814.1:n.62+41249G>A
|
|
NM_004938.4:c.62+41249G>A
MANE Select
|
NP_004929.2:n.62+41249G>A
|
|
NM_001288730.2:c.62+41249G>A
|
NP_001275659.1:n.62+41249G>A
|
|
NM_001288731.2:c.62+41249G>A
|
NP_001275660.1:n.62+41249G>A
|
|
NM_001288729.2:c.62+41249G>A
|
NP_001275658.1:n.62+41249G>A
|
|